Developmental aspects of long QT syndrome type 3 and brugada syndrome on the basis of a single SCN5A mutation in childhood

Journal of the American College of Cardiology

Volumn 46, Issue 2, 2005, Pages 331-337

  Beaufort Krol, Gertie C M ^a   Van Den Berg, Maarten P ^b   Wilde, Arthur A M ^d   Van Tintelen, J Peter ^c   Viersma, Jan Willem ^b   Bezzina, Connie R ^d   Bink Boelkens, Margreet Th E ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^c Clinical Genetics   (Netherlands)

^d ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; BRADYCARDIA; BRUGADA SYNDROME; CHILD; CHILDHOOD; CORRELATION ANALYSIS; DEVELOPMENTAL GENETICS; DIAGNOSTIC PROCEDURE; ELECTROCARDIOGRAM; FEMALE; GENE MUTATION; HEART RATE; HOLTER MONITORING; HUMAN; HYPERTENSION; INFANT; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; SEX DIFFERENTIATION; ST SEGMENT ELEVATION;

ADOLESCENT; ADULT; AGE OF ONSET; BUNDLE-BRANCH BLOCK; CHILD; CHILD, PRESCHOOL; DEATH, SUDDEN, CARDIAC; ELECTROCARDIOGRAPHY; ELECTROCARDIOGRAPHY, AMBULATORY; EXERCISE TEST; FEMALE; HEART RATE; HETEROZYGOTE; HUMANS; INFANT; LONG QT SYNDROME; MALE; MUTATION; PEDIGREE; PHENOTYPE; RISK; SENSITIVITY AND SPECIFICITY; SODIUM CHANNELS;

EID: 22044453803     PISSN: 07351097     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jacc.2005.03.066     Document Type: Article

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