Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations.

Author:

Fanin M,Duggan D J,Mostacciuolo M L,Martinello F,Freda M P,Soraru G,Trevisan C P,Hoffman E P,Angelini C

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference38 articles.

1. The limb-girdle muscular dystrophies. Proposal for a new nomenclature;Bushby, K.M.D.; Beckmann, J.S.;Neuromusc Disord,1995

2. A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage analysis;Beckmann, J.S.; Richard, I.; Hillaire, D.;C R Acad Sci Paris,1991

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

4. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q;KB, Ben Othmane; M, Ben Hamida; MA, Pericak-Vance,1992

5. Human adhalin is alternatively spliced and the gene is located;McNally, E.M.; Yoshida, M.; Mizuno, Y.,1994

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