Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome

Canadian Journal of Physiology and Pharmacology

Volumn 81, Issue 2, 2003, Pages 129-134

  Deschênes, Dominic ^a,b   Acharfi, Said ^a,b   Pouliot, Valerie ^a,b   Hegele, Robert ^c   Krahn, Andrew ^c   Daleau, Pascal ^a,b   Chahine, Mohamed ^a,b,d  

^a UNIVERSITÉ LAVAL   (Canada)

^b LAVAL UNIVERSITY   (Canada)

^c ROBARTS RESEARCH INSTITUTE   (Canada)

^d LAVAL UNIVERSITY   (Canada)

Author keywords

KCNQ1; Long QT syndrome; Potassium channels; Ventricular fibrillation

Indexed keywords

COMPLEMENTARY DNA; ION CHANNEL; POTASSIUM CHANNEL;

ANIMAL CELL; CHO CELL; CONFERENCE PAPER; GENE MUTATION; GENETIC TRANSFECTION; HEART DISEASE; HEART REPOLARIZATION; HEART VENTRICLE FIBRILLATION; LONG QT SYNDROME; NONHUMAN; PATCH CLAMP; POTASSIUM CURRENT; PRIORITY JOURNAL; PROTEIN EXPRESSION; SUDDEN DEATH; SYNCOPE;

ADOLESCENT; ANIMALS; BIOPHYSICS; CHO CELLS; CRICETINAE; CRICETULUS; DELAYED RECTIFIER POTASSIUM CHANNELS; HUMANS; KCNQ POTASSIUM CHANNELS; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; MALE; MUTATION; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED; TRANSFECTION;

EID: 0037307416     PISSN: 00084212     EISSN: None     Source Type: Journal    
DOI: 10.1139/y02-162     Document Type: Conference Paper

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