Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1-Reference-Cited by-同舟云学术

Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1

Published:2008-01-29 Issue:2 Volume:132 Page:452-464
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Schessl Joachim,Taratuto Ana L.,Sewry Caroline,Battini Roberta,Chin Steven S.,Maiti Baijayanta,Dubrovsky Alberto L.,Erro Marcela G.,Espada Graciela,Robertella Monica,Saccoliti Maria,Olmos Patricia,Bridges Leslie R.,Standring Peter,Hu Ying,Zou Yaqun,Swoboda Kathryn J.,Scavina Mena,Goebel Hans-Hilmar,Mitchell Christina A.,Flanigan Kevin M.,Muntoni Francesco,Bönnemann Carsten G.

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/132/2/452/13734764/awn325.pdf

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3. Characterization of two isoforms of the skeletal muscle LIM protein 1, SLIM1. Localization of SLIM1 at focal adhesions and the isoform slimmer in the nucleus of myoblasts and cytoplasm of myotubes suggests distinct roles in the cytoskeleton and in nuclear-cytoplasmic communication;Brown;J Biol Chem,1999

4. New observations in reducing body myopathy;Carpenter;Neurology,1985

5. DeLIMiting development;Curtiss;Bioessays,1998

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