Transient receptor potential cation channels in normal and dystrophic mdx muscle-Reference-Cited by-同舟云学术

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Transient receptor potential cation channels in normal and dystrophic mdx muscle

Published:2008-06 Issue:6 Volume:18 Page:501-513
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Krüger Jana,Kunert-Keil Christiane,Bisping Frederike,Brinkmeier Heinrich

Publisher

Elsevier BV

Subject

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

Reference57 articles.

1. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987

2. Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage;Campbell;Cell,1995

3. Refining the clinical picture;Emery,1995

4. The animal models of Duchenne muscular dystrophy: windows on the pathophysiological consequences of dystrophin deficiency;Hoffman;Curr Top Membr,1991

5. 76th ENMC international workshop: pathophysiology and therapy in the mdx mouse 21–23 January 2000, Naarden, The Netherlands;Rüdel;Neuromuscul Disord,2002

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