Autosomal-Dominant Distal Myopathy Associated with a Recurrent Missense Mutation in the Gene Encoding the Nuclear Matrix Protein, Matrin 3-Reference-Cited by-同舟云学术

Autosomal-Dominant Distal Myopathy Associated with a Recurrent Missense Mutation in the Gene Encoding the Nuclear Matrix Protein, Matrin 3

Published:2009-04 Issue:4 Volume:84 Page:511-518
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Senderek Jan,Garvey Sean M.,Krieger Michael,Guergueltcheva Velina,Urtizberea Andoni,Roos Andreas,Elbracht Miriam,Stendel Claudia,Tournev Ivailo,Mihailova Violeta,Feit Howard,Tramonte Jeff,Hedera Peter,Crooks Kristy,Bergmann Carsten,Rudnik-Schöneborn Sabine,Zerres Klaus,Lochmüller Hanns,Seboun Eric,Weis Joachim,Beckmann Jacques S.,Hauser Michael A.,Jackson Charles E.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference52 articles.

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4. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy;Liu;Nat. Genet.,1998

5. Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy;Tateyama;Neurology,2002

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