Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation-Reference-Cited by-同舟云学术

Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation

Published:2010-01 Issue:1 Volume:67 Page:136-140
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Knoblauch Hans,Geier Christian,Adams Stephanie,Budde Birgit,Rudolph André,Zacharias Ute,Schulz-Menger Jeannette,Spuler Andreas,Yaou Rabah Ben,Nürnberg Peter,Voit Thomas,Bonne Gisele,Spuler Simone

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.21839/fullpdf

Reference10 articles.

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

2. An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1;Windpassinger;Am J Hum Genet,2008

3. X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1;Quinzii;Am J Hum Genet,2008

4. Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy;Cowling;J Cell Biol,2008

5. Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosis;Voit;Neuropediatrics,1988

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