Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome

Heart Rhythm

Volumn 1, Issue 1, 2004, Pages 60-64

  Khositseth, Anant ^a   Tester, David J ^a   Will, Melissa L ^a   Bell, Carla M ^a   Ackerman, Michael J ^a,b  

^a Mayo Clinic   (United States)

^b MAYO GRADUATE SCHOOL   (United States)

Author keywords

Genetic testing; Long QT syndrome; Postpartum period; Sudden death

Indexed keywords

GENE PRODUCT; POTASSIUM CHANNEL HERG; POTASSIUM CHANNEL KCNQ1;

ADULT; AUDITORY STIMULATION; CARDIOVERSION; COHORT ANALYSIS; CONTROLLED STUDY; DEFIBRILLATION; DELIVERY; FAMILY HISTORY; FEMALE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENOTYPE; HEART ARREST; HEART ARRHYTHMIA; HEART VENTRICLE FIBRILLATION; HUMAN; INTERVIEW; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MEDICAL RECORD; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; PUERPERIUM; REVIEW; SUDDEN DEATH; SWIMMING; SYNCOPE; TELEPHONE;

EID: 2442532568     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2004.01.006     Document Type: Article

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