Permanent myopathy caused by mutation of SCN4A Metl592Val: Observation on myogenesis in vitro and on effect of basic fibroblast growth factor on the muscle

Neuroscience Bulletin

Volumn 25, Issue 2, 2009, Pages 61-66

  Feng, Yu ^a   Wang, Hong ^a   Luo, Xiao Guang ^a   Ren, Yan ^a  

^a CHINA MEDICAL UNIVERSITY   (China)

Author keywords

Basic fibroblast growth factor; Cell culture; Permanent myopathy; SCN4A

Indexed keywords

BASIC FIBROBLAST GROWTH FACTOR; CREATINE KINASE; LACTATE DEHYDROGENASE; PROTEIN;

ADULT; ARTICLE; BONE INJURY; CASE REPORT; CELL CULTURE; CELL MATURATION; CELL PROLIFERATION; CHINESE; CHROMOSOME 17Q; CONTROLLED STUDY; DOSE RESPONSE; GASTROCNEMIUS MUSCLE; GENE MUTATION; GENETIC SCREENING; HUMAN; HUMAN TISSUE; IN VITRO STUDY; MALE; MUSCLE CELL; MUSCLE DEVELOPMENT; MYOPATHY; NOMOKALAEMIC PERIODIC PARALYSIS; PARALYSIS; SKELETAL MUSCLE VOLTAGE GATED SODIUM CHANNEL GENE;

ADULT; CELL PROLIFERATION; CELLS, CULTURED; CREATINE KINASE; DOSE-RESPONSE RELATIONSHIP, DRUG; FIBROBLAST GROWTH FACTOR 2; HUMANS; L-LACTATE DEHYDROGENASE; MALE; METHIONINE; MIDDLE AGED; MUSCLE DEVELOPMENT; MUSCULAR DISEASES; MUTATION; MYOBLASTS; SODIUM CHANNELS; VALINE;

EID: 63049118196     PISSN: 16737067     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12264-009-0926-2     Document Type: Article

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