Four and a half LIM protein 1 gene mutations cause four distinct human myopathies: A comprehensive review of the clinical, histological and pathological features-Reference-Cited by-同舟云学术

Four and a half LIM protein 1 gene mutations cause four distinct human myopathies: A comprehensive review of the clinical, histological and pathological features

Published:2011-04 Issue:4 Volume:21 Page:237-251
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Cowling Belinda S.,Cottle Denny L.,Wilding Brendan R.,D’Arcy Colleen E.,Mitchell Christina A.,McGrath Meagan J.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

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3. Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy;Geier;Hum Mol Genet,2008

4. Genotype–phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin;Bos;Mol Genet Metab,2006

5. Decreased interactions of mutant muscle LIM protein (MLP) with N-RAP and alpha-actinin and their implication for hypertrophic cardiomyopathy;Gehmlich;Cell Tissue Res,2004

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