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Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12
by
Azlbi, Kemal
,
Bachner, Luclen
,
S.Beckmann, Jacques
,
Matsumura, Kllchlro
,
Hamouda, Elhadl
,
Chaouch, Mallka
,
Chaouch, Athmane
,
Alt-Ouarab, Rachlda
,
Vlgnal, Alaln
,
Welssenbach, Jean
,
Vinet, Marie-Claude
,
Leturcq, France
,
Collln, Huguette
,
M.S.Tomé, Fernando
,
Reghis, Abderrezak
,
Fardeau, Michel
,
P.Campbell, Kevin
,
Kaplan, Jean-Claude
Published in
Human molecular genetics
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Hum Mol Genet
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Human Molecular Genetics
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Biochemistry & Molecular Biology
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Biological And Medical Sciences
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Child
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Chromosome 13
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Chromosome Mapping
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Chromosomes, Human, Pair 13
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Consanguinity
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Cytoskeletal Proteins - Deficiency
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Cytoskeletal Proteins - Genetics
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Diseases Of Striated Muscles. Neuromuscular Diseases
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Dystrophin-Associated Glycoprotein
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Female
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Genes
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Genes, Recessive
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Genetic Linkage
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Genetics & Heredity
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Humans
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Immunohistochemistry
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Life Sciences & Biomedicine
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Male
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Oxford Journals Online
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Oxford University Press:jisc Collections:oxford Journal Archive: Access Period 2024-2025
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