A novel SCN5A mutation associated with the linker between III and IV domains of Nav1.5 in a neonate with fatal long QT syndrome

International Journal of Cardiology

Volumn 145, Issue 1, 2010, Pages 61-64

  Yamamura, Kenichiro ^a   Muneuchi, Jun ^a   Uike, Kiyoshi ^a   Ikeda, Kazuyuki ^a   Inoue, Hirosuke ^a   Takahata, Yasushi ^a   Shiokawa, Yuichi ^a   Yoshikane, Yukako ^b   Makiyama, Takeru ^c   Horie, Minoru ^d   Hara, Toshiro ^a  

^a KYUSHU UNIVERSITY   (Japan)

^b FUKUOKA UNIVERSITY HOSPITAL   (Japan)

^c KYOTO UNIVERSITY   (Japan)

^d SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

Author keywords

Fetal arrhythmia; Linker of III IV domains; Long QT syndrome; SCN5A

Indexed keywords

UNCLASSIFIED DRUG; VOLTAGE GATED SODIUM CHANNEL; VOLTAGE GATED SODIUM CHANNEL 1.5;

ATRIOVENTRICULAR BLOCK; CASE REPORT; ELECTROCARDIOGRAM; FATALITY; GENE; GENE MUTATION; HEART DEATH; HEART VENTRICLE TACHYCARDIA; HUMAN; LETTER; LONG QT SYNDROME; MALE; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DOMAIN; QT INTERVAL; SCN5A GENE; SEQUENCE ANALYSIS;

EID: 78049486203     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2009.04.023     Document Type: Article

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