Hereditary myosin myopathies

Neuromuscular Disorders

Volumn 17, Issue 5, 2007, Pages 355-367

  Oldfors, Anders ^a  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Actin; Genes; Mutations; Myosin; Myosin heavy chain

Indexed keywords

GENE PRODUCT; MYOSIN; MYOSIN HEAVY CHAIN BETA; MYOSIN IIA; MYOSIN III; MYOSIN VII; MYOSIN VIII; UNCLASSIFIED DRUG;

ANKLE; ARTHROGRYPOSIS; AUTOSOMAL DOMINANT INHERITANCE; CELL VACUOLE; CHILDHOOD DISEASE; CLINICAL FEATURE; CONGESTIVE CARDIOMYOPATHY; DISTAL MYOPATHY; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC VARIABILITY; HEREDITARY SPINAL MUSCULAR ATROPHY; HISTOPATHOLOGY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; HYPOPITUITARISM; JOINT CONTRACTURE; MISSENSE MUTATION; MOBILIZATION; MOLECULAR GENETICS; MORPHOLOGICAL TRAIT; MUSCLE DEVELOPMENT; MUSCLE DISEASE; MUSCLE WEAKNESS; MYOPATHY; OPHTHALMOPLEGIA; PATHOGENESIS; PRIORITY JOURNAL; REVIEW; SKELETAL MUSCLE; SLOW MUSCLE; STORAGE; TOE;

HUMANS; MODELS, BIOLOGICAL; MODELS, MOLECULAR; MUSCLE, SKELETAL; MUSCULAR DISEASES; MUTATION; MYOSIN HEAVY CHAINS;

EID: 34247554304     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2007.02.008     Document Type: Review

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