Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes

Journal of Molecular and Cellular Cardiology

Volumn 48, Issue 5, 2010, Pages 1007-1013

  Armel, Thomas Z ^a   Leinwand, Leslie A ^a  

^a UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

Author keywords

Dilated cardiomyopathy; Distal myopathy; LMM; MPD1; Myosin

Indexed keywords

AMINO ACID; MYOSIN HEAVY CHAIN BETA;

ALPHA HELIX; ARTICLE; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; DISTAL MYOPATHY; GENE MUTATION; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ASSEMBLY; THERMODYNAMICS;

AMINO ACIDS; CALORIMETRY, DIFFERENTIAL SCANNING; CARDIOMYOPATHY, DILATED; CIRCULAR DICHROISM; DISTAL MYOPATHIES; HUMANS; MICROFILAMENTS; MICROSCOPY, ELECTRON; MODELS, BIOLOGICAL; MUTATION; MYOSIN SUBFRAGMENTS; MYOSINS; PROTEIN STABILITY; STRUCTURE-ACTIVITY RELATIONSHIP; THERMODYNAMICS;

EID: 77951623814     PISSN: 00222828     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.yjmcc.2009.10.011     Document Type: Article

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