Nemaline myopathy: A clinical study of 143 cases-Reference-Cited by-同舟云学术

Nemaline myopathy: A clinical study of 143 cases

Published:2001 Issue:3 Volume:50 Page:312-320
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Ryan Monique M.,Schnell Christina,Strickland Corinne D.,Shield Lloyd K.,Morgan Graeme,Iannaccone Susan T.,Laing Nigel G.,Beggs Alan H.,North Kathryn N.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference37 articles.

1. Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy.

2. Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy

3. Report of the 70th ENMC International Workshop: Nemaline myopathy, 11–13 June 1999, Naarden, The Netherlands

4. A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

5. Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

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