A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation

Journal of Clinical Investigation

Volumn 106, Issue 3, 2000, Pages 431-438

  Bendahhou, Saïd ^a   Cummins, Theodore R ^b,c   Hahn, Angelika F ^d   Langlois, Sylvie ^e   Waxman, Stephen G ^b,c   Ptácek, Louis J ^a,f  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c VA CONNECTICUT HEALTHCARE SYSTEM   (United States)

^d UNIVERSITY OF WESTERN ONTARIO   (Canada)

^e BC CHILDREN S HOSPITAL   (Canada)

^f HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ISOLEUCINE; LEUCINE; METHIONINE; PHENYLALANINE; SODIUM CHANNEL; SODIUM ION;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CONTROLLED STUDY; EMBRYO; GENE MUTATION; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN CELL; KIDNEY CELL; MALE; MALIGNANT HYPERTHERMIA; NUCLEIC ACID BASE SUBSTITUTION; PERIODIC PARALYSIS; PRIORITY JOURNAL;

EID: 0033842533     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI9654     Document Type: Article

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