NovelFHL1mutation in a family with reducing body myopathy-Reference-Cited by-同舟云学术

NovelFHL1mutation in a family with reducing body myopathy

Published:2012-11-21 Issue:1 Volume:47 Page:127-134
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Schreckenbach Tobias,Henn Wolfram,Kress Wolfram,Roos Andreas,Maschke Matthias,Feiden Wolfgang,Dillmann Ulrich,Schulz Jörg B.,Weis Joachim,Claeys Kristl G.

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference23 articles.

1. Reducing body myopathy;Brooke;Neurology,1972

2. Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy;Schessl;J Clin Invest,2008

3. Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1;Schessl;Brain,2009

4. Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1;Schessl;Neuropediatrics,2010

5. Novel FHL1 mutations in fatal and benign reducing body myopathy;Shalaby;Neurology,2009

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