Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy-Reference-Cited by-同舟云学术

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

Published:1994-08 Issue:4 Volume:78 Page:625-633
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Roberds Steven L.,Leturcq France,Allamand Valérie,Piccolo Federica,Jeanpierre Marc,Anderson Richard D.,Lim Leland E.,Lee Jane C.,Tomé Fernando M.S.,Romero Norma B.,Fardeau Michel,Beckmann Jacques S.,Kaplan Jean-Claude,Campbell Kevin P.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference47 articles.

1. Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution;Adams;Neuron,1993

2. Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12;Azibi;Hum. Mol. Genet.,1993

3. A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p;Bashir;Hum. Mol. Genet.,1994

4. A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage;Beckmann;CR Aced. Sci. (Paris),1991

5. Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia;Ben Hamida;Muscle Nerve,1983

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