Skeletal muscle myopathy mutations at the actin tropomyosin interface that cause gain- or loss-of-function

Journal of Muscle Research and Cell Motility

Volumn 34, Issue 3-4, 2013, Pages 165-169

  Memo, Massimiliano ^a   Marston, Steven ^a  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

Author keywords

Actin; Ca2+ sensitivity; Myopathy; Skeletal muscle; Tropomyosin

Indexed keywords

ACTIN; TROPOMYOSIN;

ACTIN FILAMENT; AMINO ACID SEQUENCE; ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; GENETICS; HUMAN; METABOLISM; MOLECULAR GENETICS; MUSCLE DISEASE; MUTATION; PHYSIOLOGY; SKELETAL MUSCLE;

ACTIN CYTOSKELETON; ACTINS; AMINO ACID SEQUENCE; HUMANS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUSCLE, SKELETAL; MUSCULAR DISEASES; MUTATION; TROPOMYOSIN;

EID: 84890127123     PISSN: 01424319     EISSN: 15732657     Source Type: Journal    
DOI: 10.1007/s10974-013-9344-y     Document Type: Article

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