A novel sodium channel mutation in a family with hypokalemic periodic paralysis

Neurology

Volumn 53, Issue 9, 1999, Pages 1932-1936

  Bulman, Dennis E ^a,b   Scoggan, K A ^b   Van Oene, M D ^a   Nicolle, M W ^a   Hahn, A F ^a   Tollar, L L ^a   Ebers, G C ^a  

^a LONDON HEALTH SCIENCES CENTRE   (Canada)

^b OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

Author keywords

Family study; Hypokalemic periodic paralysis; Mutation; SCNA4

Indexed keywords

SODIUM CHANNEL;

ADULT; AMINO ACID SEQUENCE; ARTICLE; CASE REPORT; GENE MUTATION; HUMAN; HYPOKALEMIC PERIODIC PARALYSIS; MALE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0032801833     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.53.9.1932     Document Type: Article

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