Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy-Reference-Cited by-同舟云学术

Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy

Published:2014-05 Issue:5 Volume:24 Page:431-435
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Couthouis Julien,Raphael Alya R.,Siskind Carly,Findlay Andrew R.,Buenrostro Jason D.,Greenleaf William J.,Vogel Hannes,Day John W.,Flanigan Kevin M.,Gitler Aaron D.

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference24 articles.

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

3. 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

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

5. Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy;Harms;Ann Neurol,2012

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