Gene mutations associated with atrioventricular block complicated by long QT syndrome

Circulation Journal

Volumn 74, Issue 12, 2010, Pages 2546-2547

  Nishizaki, Mitsuhiro ^a   Hiraoka, Masayasu ^b  

^a Yokohama Minami Kyosai Hospital   (Japan)

^b TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL HERG; POTASSIUM CHANNEL KCNE1; POTASSIUM CHANNEL KCNE2; POTASSIUM CHANNEL KCNQ1; SODIUM CHANNEL NAV1.5;

AFTERHYPERPOLARIZATION; ARTIFICIAL HEART PACEMAKER; ATRIOVENTRICULAR BLOCK; DISEASE SEVERITY; EDITORIAL; FAMILY HISTORY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CODE; GENETIC POLYMORPHISM; GENETIC SCREENING; HEART ARREST; HEART PACING; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; LONG QT SYNDROME; LOSS OF FUNCTION MUTATION; MISSENSE MUTATION; MUTATIONAL ANALYSIS; PATHOGENESIS; PHENOTYPE; QT PROLONGATION; RECURRENT DISEASE; SINUS BRADYCARDIA; SYNCOPE; TORSADE DES POINTES;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; ANIMALS; ATRIOVENTRICULAR BLOCK; CHO CELLS; COHORT STUDIES; COMPUTER SIMULATION; CRICETINAE; CRICETULUS; ETHER-A-GO-GO POTASSIUM CHANNELS; FEMALE; HUMANS; ION CHANNEL GATING; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; MALE; MIDDLE AGED; MUTATION, MISSENSE; TORSADES DE POINTES;

EID: 78649706757     PISSN: 13469843     EISSN: 13474820     Source Type: Journal    
DOI: 10.1253/circj.CJ-10-1017     Document Type: Editorial

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