Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes
Year: 2009
Type: article
Authors: Thomas Z. Armel, Leslie A. Leinwand
Institution: University of Colorado Boulder
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W2039411908
