Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy-Reference-Cited by-同舟云学术

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Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy

Published:2012-02-14 Issue:3 Volume:71 Page:407-416
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Harms Matthew B.,Sommerville R. Brian,Allred Peggy,Bell Shaughn,Ma Duanduan,Cooper Paul,Lopate Glenn,Pestronk Alan,Weihl Conrad C.,Baloh Robert H.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference51 articles.

1. Diagnostic criteria for the limb-girdle muscular dystrophies: report of the ENMC Consortium on Limb-Girdle Dystrophies;Bushby;Neuromuscul Disord,1995

2. Pestronk A http://neuromuscular.wustl.edu/musdist/lg.html 2011

3. Myotilin is mutated in limb girdle muscular dystrophy 1A;Hauser;Hum Mol Genet,2000

4. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B);Muchir;Hum Mol Genet,2000

5. Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy;Minetti;Nat Genet,1998

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