Mutations inTPM3are a common cause of congenital fiber type disproportion-Reference-Cited by-同舟云学术

Mutations inTPM3are a common cause of congenital fiber type disproportion

Published:2008-03 Issue:3 Volume:63 Page:329-337
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Clarke Nigel F.,Kolski Hanna,Dye Danielle E.,Lim Esther,Smith Robert L. L.,Patel Rakesh,Fahey Michael C.,Bellance Rémi,Romero Norma B.,Johnson Edward S.,Labarre-Vila Annick,Monnier Nicole,Laing Nigel G.,North Kathryn N.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.21308/fullpdf

Reference28 articles.

1. Congenital fiber type disproportion-30 years on;Clarke;J Neuropathol Exp Neurol,2003

2. The significance of type 1 fiber atrophy (hypotrophy) in childhood neuromuscular disorders;Imoto;Brain Dev,2001

3. Actin mutations are one cause of congenital fibre type disproportion;Laing;Ann Neurol,2004

4. A novel X-linked form of congenital fibre type disproportion;Clarke;Ann Neurol,2005

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