The long-QT syndrome - Bedside to bench to bedside

New England Journal of Medicine

Volumn 348, Issue 19, 2003, Pages 1837-1838

  Vincent, G Michael ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL; SODIUM CHANNEL;

ADOLESCENT; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; DISEASE COURSE; ELECTROCARDIOGRAM; GENDER; GENE MUTATION; GENETIC PREDISPOSITION; GENETIC RISK; GENOTYPE; HEART RATE; HUMAN; LONG QT SYNDROME; MALE; PHENOTYPE; PRIORITY JOURNAL; REVIEW; RISK ASSESSMENT; SUDDEN DEATH;

ADOLESCENT; ADULT; DEATH, SUDDEN, CARDIAC; ELECTROCARDIOGRAPHY; FEMALE; HETEROZYGOTE; HUMANS; LONG QT SYNDROME; MALE; MUTATION; RISK ASSESSMENT;

EID: 0038753947     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJMp030039     Document Type: Review

References (2)

1. Splawski I, Shea J, Timothy KW, et al. Spectrum of mutations in long-QT syndrome genes KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation 2000;102:1178-85.
2. Doyle DA, Morais Cabral J, Pfuetzner RA, et al. The structure of the potassium channel: molecular basis of K+ conduction and selectivity. Science 1998;280:69-77.