Melki J, Abdelhak S, Sheth P, Bachelot
MF, Burlet P et al. PUBLICATIONS
1990
1.
Melki J, Abdelhak S, Sheth P, Bachelot
MF, Burlet P et al.
Gene
for proximal
spinal muscular
atrophies maps
to chromosome
5q.
Nature
344:767-768
2.
Melki
J, Sheth P, Abdelhak S, Burlet et al.
Mapping
of acute (type I) spinal muscular atrophy to chromosome 5q12-q14.
Lancet
336:271-273
3.
Melki
J, Abdelhak S, Sheth P, Bachelot MF, Burlet P
et al.
Chromosomal
localisation of chronic proximal spinal muscular atrophies of childhood
Journal
of the Neurological Sciences 98
4.
Abdelhak
S.,Melki j, Bachelot M.F., Burlet P et al.
A
PstI polymorphism at the D5S39 locus
Nucleic
Acid Research 18:5580
5.
Melki
J, Abdelhak S, Sheth P, Bachelot MF, Burlet P et al.
Chromosomal
localisation of chronic proximal spinal muscular atrophies of childhood
Journal
of Neurology 237
6.
Melki J, Abdelhak S, Sheth P, Bachelot MF, Burlet
P, et al.
Chromosomal localisation of chronic proximal spinal
muscular atrophies of childhood
Second Meeting of the European Neurological Society
7.
Melki J, Sheth P, Abdelhak S, Burlet P, Bachelot MF, Lathrop M, Frezal J, et al.
Mapping of the childhood spinal muscular atrophy locus
to chromosome 5q12-q14.
American Journal of Human Genetics
47:3;1401
1991
8.
Sheth P., Abdelhak S., Bachelot M.F., Burlet
P et al.
Linkage analysis in spinal muscular atrophy, by six
closely flanking markers on chromosome 5.
Am. J. Hum. Genet. 48:764-768.
9.
Mattei
M.G., Melki j., Bachelot M.F., Abdelhak S., Burlet P. et al.
In
situ hybridisation of two markers closely flanking the SMA gene to 5q12-q13.3
Cyto
Genet and Cell Genet 57: 112-113
10.
Abdelhak
S., Burlet P. et al.
Generation of new DNA probes in the vicinity of the SMA
locus
Human Gene mapping 27443
11.
Melki
j., Abdelhak S., Burlet P. et al.
Prenatal diagnosis of SMA using polymorphic DNA probes
of the 5q12-q14 region
Human Gene mapping 27444
12.
Abdelhak
S., Burlet P. et al.
Generation of new DNA probes in the vicinity of the SMA
locus
International congress of Human genetics
2101
13.
Melki
j., Abdelhak S., Burlet P. et al.
Cartographie
génétique des amyotrophies spinales de l’enfant
Colloque
National sur les Maladies Neuromusculaires p 11
14.
Abdelhak
S., Burlet P. et al.
Generation of new DNA probes in the vicinity of the SMA
locus
Colloque
National sur les Maladies Neuromusculaires p 80
15.
Melki
j., Abdelhak S., Burlet P. et al.
Prenatal diagnosis of SMA using polymorphic DNA probes
of the 5q12-q14 region
Colloque
National sur les Maladies Neuromusculaires p 370
1992
16.
Melki, J., Burlet P.
et al.
High
resolution genetic map of new DNA markers closely flanking the SMA locus
Cyto
Genet and Cell Genet 61: 233
17.
Melki
J, Abdelhak S, Burlet P et al.
Prenatal
prediction of Werdnig-Hoffmann disease
Journal
of medical Genetics 29:171-174
18.
Muller B, Melki J,
Burlet P et al.
Proximal
SMA type II and III in the same sibship are not caused by different alleles
Am.
J. Hum. Genet. 50:892-895
19.
Melki
J, Burlet P et al .
High resolution genetic map of new DNA markers closely
flanking the SMA locus
International workshop on chromosome 5
20.
Muller
B, Melki J, Burlet P et al .
No evidence for allelic heterogeneity between SMA type
II and III at the SMA locus
European Society of Human Genetics 210
21.
Melki J, Abdelhak S, Burlet P et al .
Clinical and molecular genetics of SMA
European Society of Human Genetics 196
22.
Sequeiros, Manaia, Silveira, Coutinho, Loureiro, Melki,
Rozet, Burlet et al.
Linkage analysis of Machado-Joseph.
Am. J. Hum. Genet. 51:1470
23.
Melki
J, Burlet P et al .
Physical map around the spinal muscular atrophy locus
using yeast artificial chromosomes.
Am. J. Hum. Genet. 51:953
1993
24.
Melki, J., Burlet P
et al.
Refined
linkage map of chromosome 5 in the region of the spinal muscular atrophy gene.
Genomics 15: 521-524.
25.
Burlet P
et al.
Trinucleotide
repeat polymorphism at the D5S556 locus .
Human
Molecular genetics 2:1328
26.
Silveira I, Manaia A, Melki J, Magarino C, Lunkes A,
Hernandez A, Gispert S, Burlet P et
al.
Machado-Joseph disease is genetically different from
Holguin Dominant Ataxia
Genomics
17: 556-586.
27.
Melki,
J., Lefebvre S, Bürglen L, Burlet
P. et al.
Carte
génétique et physique haute resolution au locus des Amyotrophies Spinales
Colloque
National sur les Maladies Neuromusculaires p35.
28.
Clermont
O, Burlet P. et al.
Identification of new
DNA markers closely flanking the SMA locus
Colloque
National sur les Maladies Neuromusculaires p 132
29.
Lefebvre S, Bürglen L,
Burlet P.et al.
Application
de l’exon trapping pour la recherche de gènes candidats
Colloque
National sur les Maladies Neuromusculaires p 213
30.
Clermont,
O., Burlet P. et al.
Identification of new polymorphic DNA markers closely
flanking the SMA locus
Am. J. Hum. Genet. 53:987.
31.
Lefebvre S, Bürglen L, Burlet P, et al.
Cloning candidate genes from the SMA region by exon
trapping amplification
Am. J. Hum. Genet. 53:1787.
32.
Lefebvre S, Bürglen L, Burlet P, et al.
Duplication and amplification of the 5q13 spinal
muscular atrophy region
Am. J. Hum. Genet. 53:1329.
1994
33.
Sequeiros
J, Silveira I, Maciel P, Coutinho P, Manaia A, Gaspar C, Burlet P et al.
Genetic
Linkage studies of Machado-Joseph.
Genomics
21:645-652
34.
Melki
J, Lefebvre S, Bürglen L, Burlet P et
al.
Physical
study of big fragments and search strategy of genes. Application to locus of
infant spinal muscular atrophies.
C
R Seances Soc Biol Fil . 188:495-8
35.
Melki
J, Lefebvre S, Bürglen L, Burlet P et al.
De
novo and inherited deletions of the
5q13 region in spinal muscular atrophies.
Science 264:1474-1477
36.
Melki
J, Lefebvre S, Bürglen L, Burlet P et
al
Délétions héritées
et de novo dans les Amyotrophies
Spinales
Médecine:Sciences
10:889-891
37.
Clermont, O., Burlet
P.et al.
Use of genetic and physical mapping to locate the spinal
muscular atrophy locus
European society of Human Genetics
502
38.
Melki J, Lefebvre S, Bürglen L, Burlet P, et al
De novo and
inherited deletions of the 5q13 region in spinal muscular atrophies.
European society of Human Genetics
338
39.
Lefebvre S., Burglen L., Clermont, O., Reboulet S, Burlet
P et al.
Identification of a gene from the SMA 5q13
region
European society of Human Genetics
338
40.
Lefebvre S., Burglen L., Zeviani M, Burlet
P., Pascal F.et al.
Cloning genes from the SMA region using the exon
trapping system
European society of Human Genetics
31
41.
Clermont,
O., Burlet P.et al.
Use
of genetic and physical mapping to locate the spinal muscular atrophy locus
between two new highly polymorphic DNA markers.
Am.
J. Hum. Genet. 54:687-694.
42.
Lefebvre S, Reboullet S, Benichou B, Bürglen L,
Clermont O, Burlet P, et al.
Isolation and characterization of candidate genes of the
5q13 region
Am. J. Hum. Genet. 54:1538.
43.
Bürglen L, Lefebvre S, Burlet P et al.
Deletion mapping of the SMA region
Am. J. Hum. Genet. 55:1491
1995
44.
Lefebvre
S, Bürglen L, Reboullet S, Clermont O, Burlet P
et al.
Identification
and characterization of a spinal muscular atrophy-determining gene.
Cell
80:155-165
45.
Bürglen
L, Lefebvre S, Reboullet S, Clermont O, Burlet P
et al.
Identification et
caractérisation d'un gène déterminant dans les Amyotrophies Spinales
Médecine:Sciences
11:149-151
46.
Clermont O, Burlet P
et al.
SMN
gene deletion in adult-onset spinal muscular atrophy .
The
Lancet: 346:1712
47.
Lefebvre S, Bürglen L, Viollet L,
Burlet P, et al.
Molecular genetics of SMA
Meeting of European Neurosciences 5.01
48.
Lefebvre S, Bürglen L, reboullet S, Clermont O,
Burlet P, et al.
Molecular characterization of SMA determining gene
European Society of Human Genetics
w8
49.
Lefebvre S, Bürglen L, Viollet L,
Burlet P, et al.
Molecular characterization of SMA determining gene
Genetic Society P2
50.
Clermont O, Bürglen L, Burlet P, Lefebvre S, et al.
Analyse
génétique de familles présentant des cas de SMA dans différentes branches
Club
de Clonage Positionnel p 22
51.
Lefebvre S, Bürglen L, Reboullet S, Clermont O, Burlet
P et al.
Identification and characterization of SMA determining
gene
Club
de Clonage Positionnel p 34
52.
Bürglen
L, Spiegel R, Clermont O, Burlet P, ,
et al.
Etude
de la region 5q13 dans 6 cas de SMA avec cardiopathie congénitale
Club
de Clonage Positionnel p 19
53.
Bürglen L, Lefebvre S,
Burlet P, et al.
Genomic organisaton of the human survival motor neuron
gene
Journée
scientifique de l’UFR Necker
54.
Burlet
P, et al.
Large deletions involving SMN, NAIP genes and markers
C212-272
Journée
scientifique de l’UFR Necker
55.
Clermont O, Bürglen L, Burlet P, et al.
Genetic analysis of unusual SMA pedigrees using SMN,
NAIP genes and markers C212-272
Journée
scientifique de l’UFR Necker
56.
Clermont O, Bürglen L, Burlet P, Lefebvre S, et al.
Genetic analysis of unusual pedigrees using SMN, NAIP
genes and markers C212 and C272.
Am. J. Hum. Genet. 57 :1370.
57.
Viollet L, Bürglen L, Lefebvre S, Burlet P, Clermont O, et al.
Identification, comparative mapping and developpemental
studies of the mouse homologue of the SMN gene.
Am. J. Hum. Genet. 57 :864.
58.
Lefebvre S, Bürglen L,
Burlet P, et al.
Immunodetection of the survival motor neuron gene
products (SMN) in controls and SMA patients.
Am. J. Hum. Genet. 57 828.
59.
Melki J, Burlet P,
Bürglen L, Clermont O, Lefebvre S et al.
Large deletions involving SMN, NAIP genes and markers
C212-272
Am. J. Hum. Genet. 57 142
60.
Bürglen L, Lefebvre S, Clermont O, Burlet P, Viollet L et al.
Genomic organisation of the human survival motor neurone
gene.
Am. J. Hum. Genet. 57 :799.
61.
Burlet
P, et al.
Etude
comparative des gènes SMN et NAIP dans les SMA
EPHE
62.
Clermont
O, Burglen L, Burlet P, et al.
Analyse
génétique de familles présentant des cas de SMA dans différentes branches.
EPHE
1996
63.
Bürglen
L, Lefebvre S, Clermont O, Burlet P et al.
Structure
and organisation of the human survival motor neurone gene.
genomics. 32:479-482
64.
Burlet P
et al.
Large
scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease.
Journal
of Medical Genetics. 33:281-283
65.
Bürglen L, Amiel J,
Viollet L, Lefebvre S, Burlet P et al.
SMN
gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy
association.
Journal
of clinical investigation.98:1130-1132
66.
Bertrandy S, Lefebvre S, Burlet P et al.
Approche
moleculaire d´une degenerescence du motoneurone spinal : Les maladies de
Werdnig-Hoffmann et de Kugelberg- Welander.
Annales
de l´Institut Pasteur. 7:187-192
67.
Lefebvre S, Burlet
P et al.
Strong correlation between the SMN protein level and SMA
phenotypes.
American Journal of Human Genetics. 59:1550
68.
Viollet L, Bertrandy S, Brunialti A, Lefebvre S,
Clermont O, Burlet P et al.
The mouse survival motor neuron gene. cDNA isolation,
expression and chromosome mapping.
American Journal of Human Genetics. 59:913
69.
Bürglen L, Seroz T., Miniou P., Lefebvre S, Burlet
P, et al.
The gene encoding P44, a subunit of the transcription
factor TFIIH is involved in large scale deletions associated with
Werdnig-Hoffmann disease.
American Journal of Human Genetics. 59:822
70.
Burlet
P et al.
Large scale deletions involving NAIP and SMN are
specific to Werdnig-Hoffmann disease.
European Society of Human Genetic
5.115
71.
Burlet
P et al.
Large scale deletions involving NAIP and SMN are
specific to Werdnig-Hoffmann disease.
European Society of Human Genetic
5.115
72.
Viollet L, Lefebvre S,
Bertrandy S, Burlet P et al.
Identification, comparative mapping and developmental
studies of the mouse homologue.
European Society of Human Genetic
9.005
73.
Bürglen L, Lefebvre S, Burlet P L et al.
genomic organisation of the human survival motor neurone
gene.
European Society of Human Genetic
5.113
74.
Lefebvre S, Burlet
P et al.
Analyses of the SMN gene products
European Society of Human Genetic
5.116
75.
Clermont O, Bürglen L, Burlet P et al.
Genetic analyses of unusual pedigrees
European Society of Human Genetic
5.117
76.
Lefebvre S, Bürglen L, Burlet P et al.
Molecular genetic of SMA
Human Gene Mapping 96
77.
Bürglen
L, Amiel J, Viollet L, Lefebvre S, Burlet
P et al.
SMN gene deletion in the arthrogryposis multiplex
congenital SMA
Neuromuscular Disorders SP21
78.
Viollet L, Bürglen L, Lefebvre S, Burlet P et al.
Identification, comparative mapping and developmental
studies of the mouse homologue.
Neuromuscular Disorders So5
79.
Lefebvre S, Burlet
P et al.
Strong correlation between the SMN protein level and SMA
phenotype
Neuromuscular Disorders So2
80.
Bürglen L, Seroz T., Miniou P., Lefebvre S, Burlet
P et al.
The gene encoding P44, a subunit of the transcription
factor TFIIH is involved in large scale deletions associated with
Werdnig-Hoffmann disease.
Neuromuscular Disorders So2
81.
Bürglen L, Seroz T., Miniou P., Lefebvre S, Burlet
P et al.
The gene encoding P44, a subunit of the transcription
factor TFIIH is involved in large scale deletions associated with
Werdnig-Hoffmann disease.
Club
de Clonage Positionnel
82.
Lefebvre
S, Burlet P et al.
Strong correlation between the SMN protein level and SMA
phenotype
Club de Clonage Positionnel
83.
Viollet L, Bertrandy S, Brunialti A, Lefebvre S,
Clermont O, Burlet P et al.
The mouse survival motor neuron gene. cDNA isolation,
expression and chromosome mapping.
Club
de Clonage Positionnel
84.
Lefebvre
S, Burlet P et al.
The SMN protein : the primary defect in SMA.
Neuromuscular Disorders in Childhood L3
85.
Lefebvre S, Bürglen L, Viollet L, Burlet P et al.
Identification and characterization of determining gene
in SMA
International workshop between Japan and France
86.
Viollet L, Bertrandy S, Brunialti A, Lefebvre S,
Clermont O, Burlet P et al.
The mouse survival motor neuron gene. cDNA isolation,
expression and chromosome mapping.
Colloque
National sur les Maladies Neuromusculaires p
327.
87.
Lefebvre S, Burlet
P, Bertrandy S, Clermont O, Bürglen L et al.
Correlation
étroite entre le taux de protéine SMn et la sévérite
Colloque
National sur les Maladies Neuromusculaires p
210.
88.
Bürglen L, Seroz T., Miniou P., Lefebvre S, Burlet
P et al.
The gene encoding P44, a subunit of the transcription
factor TFIIH is involved in large scale deletions associated with
Werdnig-Hoffmann disease.
Colloque
National sur les Maladies Neuromusculaires p
110.
89.
Melki J, Lefebvre S, Bertrandy S, Viollet L, Bürglen L
, Burlet P et al.
De
la clinique au produit du gène
Colloque
National sur les Maladies Neuromusculaires p
22.
90.
Viollet L, Bertrandy S, Brunialti A, Lefebvre S,
Clermont O, Burlet P et al.
The mouse survival motor neuron gene. cDNA isolation,
expression and chromosome mapping.
Club du motoneurone
p 22.
1997
91.
Viollet
L, Bertrandy S, Brunialti A, Lefebvre S, Clermont O, Burlet P,
et al.
cDNA
isolation, expression and chromosomal localisation of the mouse survival motor
neuron gene.
Genomics.
40:185-188
92.
Lefebvre
S, Burlet P, et al.
Correlation
between severity and SMN protein level in spinal muscular atrophy
Nature
Genetics : 16 : 265-269
93.
Bürglen
L, Seroz T., Miniou P., Lefebvre S, Burlet P, Munnich A,
Viegas-Pequignot E., Egly JM., Melki J .
The
gene encoding P44, a subunit of the transcription factor TFIIH is involved in
large scale deletions associated with Werdnig-Hoffmann disease.
American
Journal of Human Genetics. 60:72-79
94.
Burlet
P,
et al.
Immunodetection of the SMN protein
American Journal of Human Genetics. 61 : 1915
95.
Burlet
P,
et al.
Mutation analysis of the SMN gene in undeleted SMA
patients
American Journal of Human Genetics. 61 : 1923
96.
Bertrandy S, Clermont O, Burlet P, et al.
The SMN gene is conserved during evolution
American Journal of Human Genetics. 61 : 2223
97.
Lefebvre S, Burlet
P, et al.
Characterization of the ribonucleoprotein complex
containing SMN
American Journal of Human Genetics. 61 : 1013
98.
Lefebvre S, Burlet
P, et al.
the SMN protein the
primary defect in SMA
European Journal of Human
genetics s 43
1998
99.
Burlet
P, et al.
The
distribution of SMN protein complex in human fetal tissues and its alteration in
SMA
Human
Molecular genetics 7:1927-1933
100.
Burlet
P,
et al.
Immunodetection of the SMN protein in human fetal
tissues
European Journal of Human
genetics 6 : 017
101.
Bertrandy S, Clermont O, Burlet P, et al.
A putative RNA binding motif is detected by computer
search in the Zebrafish SMN gene, an orthologue of the SMA disease gene
European Journal of Human
genetics 6 : 054
102.
Bertrandy S, Clermont O, Burlet P, et al.
Recombinant SMN protein from the zebrafish ortholog of
the SMA-causing gene
American Journal of Human Genetics. 63 : 1516
103.
Burlet
P, et al.
The distribution of SMN protein complex in human fetal
tissues
American Journal of Human Genetics. 63 : 904
104.
Burlet
P,
et al.
Immunodetection of the SMN protein in human fetal
tissues
European Journal of Human
genetics 6 : 017
105.
Bertrandy S, Clermont O, Burlet P, et al.
A putative RNA binding motif is detected by computer
search in the Zebrafish SMN gene, an orthologue of the SMA disease gene
European Journal of Human
genetics 6 : 054
1999
106.
Bertrandy
S, Burlet P et al.
The
RNA binding properties of SMN
Human
Molecular genetics 8:775-782
107.
Burlet
P,
et al.
SMN protein is associated to large cytoplasmic dot like
structure in human fetal muscle
European Journal of Human
genetics 7 : 324
108.
Bertrandy S, Burlet
P, et al.
The RNA binding properties of SMN : deletion analysis of
the zebrafish ortholog defines domains conserved in evolution
European Journal of Human
genetics 7 : 441
109.
Burlet
P, et al.
Fonctional analyses of SMN/SMNc gene expression :
therapeutic implications in spinal muscular atrophy
American Journal of Human Genetics. 65 : 1729
110.
Lefebvre S, Burlet
P, et al.
The loss of function of a SMN frameshit mutation in SMA
American Journal of Human Genetics. 65
: 279
111.
Viollet
L, Barois A, Burlet P, et al.
Autosomal Recessive Distal Spinal muscular Atrophy with
diaphragmatic palsy in childhood is not linked to 5q13 SMA locus.
American Journal of Human Genetics. 65 : 2558
112.
Bertrandy S, Lefebvre S, Burlet P, et al.
Double stranded RNA-mediated genetic interference of SMN
leads to embryonic lethalithy in the nematode C. elegans
European Journal of Human
genetics 7 : 076
113.
Lefebvre S, Bertrandy S, Burlet P, et al.
The evolutionary conserved RNA binding properties of SMN
BIOCHIMIE
6 : 271
2000
114.
Burlet P,
et al.
Therapeutic implications by upregulating SMN2 expression
in Spinal Muscular Atrophy
American Journal of Human Genetics. 67-2439
115.
Lefebvre S, Bertrandy S, Burlet P, Belser C, Viollet L et al.
The loss of function of SMN frameshift mutation 472del5
in SMA
American Journal of Human Genetics. 67-210
116.
Viollet
l, Leclair-Richard D, Burlet P,
Belser C, Vial E et al.
A new varient for autosomal recessive spinal muscular
atrophy in childhood
American Journal of Human Genetics. 67-563
117.
Vial
e, Burlet P,
et al.
SMA
carrier detection using real time quantitative taq man PCR
Myologie 2000 499
118.
Lefebvre S, Bertrandy S, Burlet P, et al.
The loss of
function of SMN frameshift mutation 472del5 in SMA
Myologie
2000 492
119.
Burlet P,
et al.
Therapeutic implications in SMA by fonctional analysis
of SMN/SMNc gene expression
Myologie
2000 485
120.
Viollet
l, Barrois A, Burlet P, et al.
The locus for neonatal SMA with respiratory distress on
chromosome 11q13-q21 is candidate for autosomal recessive distal spinal muscular
atrophy with diaphragmatic palsy in childhood
Myologie 2000 500
121.
Lefebvre S, Bertrandy S, Burlet P, et al.
The loss of function of SMN frameshift mutation 472del5
in SMA
European Journal of Human
genetics p-478
122.
Burlet
P,
et al.
Therapeutic implications of SMNc protein in SMA
European Journal of Human
genetics p-738
123.
Vial
e, Burlet P,
et al.
SMA carrier detection using real time quantitative taq
man PCR
European Journal of Human
genetics p-520
124.
Viollet
l, Barrois A, Burlet P, et al.
Autosomal recessive distal SMA with diaphragmatic palsy
in childhood and SMA with respiratory distress are linked to the same locus
European Journal of Human
genetics p-669
2001
125.
Burlet
P et al.
SMN2 gene stimulations give differential expression in
SMA and control cultured cells
American Journal of Human Genetics. 69
: 2937
126.
Vial
e, Burlet P
et al.
SMA carrier detection using real time quantitative taq
man PCR
American Journal of Human Genetics. 69
: 1434
127.
Viollet
l, Burlet P et al.
Mapping of autosomal recessive distal spinal muscular
atrophy to chromosome 11q13 in a large kindred
American Journal of Human Genetics. 69 : 1863
128.
Lefebvre S, Burlet
P, et al.
A novel association of the SMN protein with two major
non-ribosomal nucleolar proteins is altered in spinal muscular atrophy
American Journal of Human Genetics. 69 : 981
129.
Lefebvre S, Burlet
P, et al.
A novel association of the SMN protein with two major
non-ribosomal nucleolar proteins is altered in spinal muscular atrophy
Familly of SMA p16
130.
Gendron N, Lefebvre S, DiDonato C, Doyle A, Burlet
P, et al.
High throughput screening for drugs upregulating SMN2
Familly of SMA p36
2002
131.
Viollet
L, Zarhate M, Burlet P
et al
Novel IGHMBP2 mutations in SMARD1
American Journal of Human Genetics. 71:670
132.
Lefebvre
S, Burlet P et al.
A
novel association of the SMN protein with two major non-ribosomal nucleolar
proteins
and its implication in spinal muscular atrophy.
Hum
Mol Genet. May 1;11(9):1017-27.
133.
Viollet L, Barois A,
Rebeiz JG, Rifai Z, Burlet P et al.
Mapping
of autosomal recessive chronic distal spinal muscular atrophy to
chromosome
11q13.
Ann
Neurol. May;51(5):585-92
134.
Viollet
L, Burlet P
et al.
Etude
génétique des amyotrophies spinales distales chroniques de l’enfant
Assises
de génétique 2002 :365, p110
2003
135.
Gigarel,
N, Burlet P, et al.
Single cell co-amplification of microsatellite markers
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