Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes
Author:
Funder
National Institutes of Health Grants
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Molecular Biology
Reference25 articles.
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5. Mutations in the beta-myosin rod cause myosin storage myopathy via multiple mechanisms;Armel;Proc. Natl. Acad. Sci. U. S. A.,2009
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