Human congenital myopathy actin mutants cause myopathy and alter Z-disc structure in Drosophila flight muscle

Neuromuscular Disorders

Volumn 23, Issue 3, 2013, Pages 243-255

  Sevdali, Maria ^a,c   Kumar, Vikash ^a,b   Peckham, Michelle ^b   Sparrow, John ^a  

^a UNIVERSITY OF YORK   (United Kingdom)

^b UNIVERSITY OF LEEDS   (United Kingdom)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Act88F; ACTA1; Actin; Drosophila; IFM; Muscle disease; Nemaline myopathy; Striated muscle

Indexed keywords

ACTIN; MUSCLE PROTEIN; TROPOMODULIN; TROPONIN I; TROPONIN T;

ACTIN FILAMENT; ARTICLE; CONGENITAL DISORDER; D154N GENE; D292V GENE; DROSOPHILA; FLIGHT MUSCLE; G15R GENE; GENE MUTATION; HETEROZYGOTE; I136M GENE; INDIRECT FLIGHT MUSCLE; MYOPATHY; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SARCOMERE; V163L GENE; V163M GENE; WILD TYPE; ZEBRA BODY; ANIMAL; FLYING; GENETICS; HUMAN; METABOLISM; MUSCLE DISEASE; PHYSIOLOGY; SKELETAL MUSCLE; TRANSGENIC ANIMAL;

ACTINS; ANIMALS; ANIMALS, GENETICALLY MODIFIED; DROSOPHILA; FLIGHT, ANIMAL; HUMANS; MUSCLE, SKELETAL; MUSCULAR DISEASES; SARCOMERES;

EID: 85027942782     PISSN: 09608966     EISSN: 18732364     Source Type: Journal    
DOI: 10.1016/j.nmd.2012.11.013     Document Type: Article

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