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Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy

Pubmed ID: 
23746549
Year: 
2013
Month: 
Jul
Volume: 
93
Issue: 
1
Citation: 
Ravenscroft G, North KN, Laing NG. Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy. American Journal of Human Genetics 93 (1) : 6 - 18(2013) PubMed