Telethonin-deficiency initially presenting as a congenital muscular dystrophy-Reference-Cited by-同舟云学术

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Telethonin-deficiency initially presenting as a congenital muscular dystrophy

Published:2011-06 Issue:6 Volume:21 Page:433-438
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Ferreiro Ana,Mezmezian Monica,Olivé Montse,Herlicoviez Danielle,Fardeau Michel,Richard Pascale,Romero Norma Beatriz

Publisher

Elsevier BV

Subject

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

Reference24 articles.

1. The congenital muscular dystrophies;Voit,2004

2. The congenital muscular dystrophies in 2004: a century of exciting progress;Muntoni;Neuromusc Disord,2004

3. 133rd ENMC International Workshop on Congenital Muscular Dystrophy (IXth International CMD Workshop) 21–23 January 2005, Naarden, The Netherlands;Muntoni;Neuromuscul Disord,2005

4. Gene table of monogenic neuromuscular disorders;Neuromusc Disord,2010

5. Mutations in the laminin alpha-2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy;Helbling-Leclerc;Nature Genet,1995

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