Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening events

Human Genetics

Volumn 131, Issue 8, 2012, Pages 1295-1304

  Chiu, Shuenn Nan ^a   Wu, Mei Hwan ^a   Su, Ming Jai ^a   Wang, Jou Kou ^a   Lin, Ming Tai ^a   Chang, Chien Chih ^a   Hsu, Hui Wen ^a   Shen, Ching Tsuen ^b   Thériault, Olivier ^c,d   Chahine, Mohamed ^c,d  

^a NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

^b CATHAY GENERAL HOSPITAL   (Taiwan)

^c CENTRE DE RECHERCHE DE L INSTITUT UNIVERSITAIRE EN SANTÉ MENTALE DE QUÉBEC   (Canada)

^d UNIVERSITÉ LAVAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CHILD; CONTROLLED STUDY; DEFIBRILLATOR; FALLOT TETRALOGY; FEMALE; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HEART VENTRICLE ARRHYTHMIA; HERG GENE; HUMAN; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MALE; OOCYTE; PRESCHOOL CHILD; PRIORITY JOURNAL; QRS COMPLEX; SCN5A GENE; SINGLE NUCLEOTIDE POLYMORPHISM; SUDDEN DEATH; XENOPUS;

ANIMALS; BASE SEQUENCE; DNA PRIMERS; FEMALE; LONG QT SYNDROME; MALE; MUTATION; POLYMORPHISM, GENETIC; TETRALOGY OF FALLOT; XENOPUS;

EID: 84864277794     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-012-1156-4     Document Type: Article

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