Phenotype variation and newcomers in ion channel disorders

Human Molecular Genetics

Volumn 6, Issue 10 REV. ISS., 1997, Pages 1679-1685

  Bulman, Dennis E ^a  

^a OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; CARRIER PROTEIN; ION CHANNEL; POTASSIUM CHANNEL; SODIUM CHANNEL; VOLTAGE GATED CHANNEL FORMING PROTEIN;

ARTICLE; ATAXIA; CELL MEMBRANE POTENTIAL; CELL SECRETION; DISEASE SEVERITY; DYSKINESIA; GENE; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC VARIABILITY; HUMAN; LONG QT SYNDROME; MIGRAINE; MOTOR DYSFUNCTION; NEUROLOGIC DISEASE; NEUROMUSCULAR DISEASE; PERIODIC PARALYSIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FAMILY; PROTEIN SECONDARY STRUCTURE; SIGNAL TRANSDUCTION; SKELETAL MUSCLE;

ANIMALS; GENETIC DISEASES, INBORN; HUMANS; ION CHANNELS; LONG QT SYNDROME; MUSCULAR DISEASES; PARALYSES, FAMILIAL PERIODIC; PHENOTYPE; POINT MUTATION; SODIUM CHANNELS; VARIATION (GENETICS);

ATAXIA;

EID: 0030806159     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.10.1679     Document Type: Article

References (8)

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