Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)-Reference-Cited by-同舟云学术

Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)

Published:2000-12 Issue:8 Volume:10 Page:553-559
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Anderson Louise V.B,Harrison Ruth M,Pogue Robert,Vafiadaki Elizabeth,Pollitt Christine,Davison Keith,Moss Jennifer A,Keers Sharon,Pyle Angela,Shaw Pamela J,Mahjneh Ibrahim,Argov Zohar,Greenberg Cheryl R,Wrogemann Klaus,Bertorini Tulio,Goebel Hans H,Beckmann Jacques S,Bashir Rumaisa,Bushby Kate M.D

Publisher

Elsevier BV

Subject

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

Reference31 articles.

1. A new locus for limb-girdle muscular dystrophy in a large consanguineous Tunisian family;Driss;Neuromusc Disord,1999

2. Making sense of the limb-girdle muscular dystrophies;Bushby;Brain,1999

3. Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A;Richard;Cell,1995

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

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