Functional effects of congenital myopathy-related mutations in gamma-tropomyosin gene

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1822, Issue 10, 2012, Pages 1562-1569

  Robaszkiewicz, Katarzyna ^a   Dudek, Elzbieta ^b,c   Kasprzak, Andrzej A ^b   Moraczewska, Joanna ^a  

^a KAZIMIERZ WIELKI UNIVERSITY   (Poland)

^b NENCKI INSTITUTE OF EXPERIMENTAL BIOLOGY   (Poland)

^c UNIVERSITY OF ALBERTA   (Canada)

Author keywords

tropomyosin; Cap disease; Congenital myopathy; Fiber type disproportion; Nemaline myopathy; Thin filament

Indexed keywords

ACTIN; ARGININE; CALCIUM ION; LYSINE; MYOSIN; MYOSIN ADENOSINE TRIPHOSPHATASE; TROPONIN;

ACTIN MYOSIN INTERACTION; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; GAMMA TROPOMYOSIN 3 GENE; GENE; GENE EXPRESSION; MISSENSE MUTATION; MUSCLE WEAKNESS; MUTANT; MYOPATHY; NEMALINE MYOPATHY; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN ISOLATION; RAT; SKELETAL MUSCLE; SLOW MUSCLE FIBER; SUBSTITUTION REACTION; THIN FILAMENT;

ACTIN CYTOSKELETON; ACTINS; ACTOMYOSIN; ADENOSINE TRIPHOSPHATASES; ANIMALS; CALCIUM; MUSCLE WEAKNESS; MUSCLE, SKELETAL; MUTATION; MYASTHENIC SYNDROMES, CONGENITAL; MYOSIN SUBFRAGMENTS; RATS; TROPOMYOSIN; TROPONIN;

EID: 84864182402     PISSN: 09254439     EISSN: 1879260X     Source Type: Journal    
DOI: 10.1016/j.bbadis.2012.06.009     Document Type: Article

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