Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

Circulation

Volumn 95, Issue 3, 1997, Pages 565-567

  Tanaka, Toshihiro ^a   Nagai, Ryozo ^b   Tomoike, Hitonobu ^c   Takata, Shigeo ^d   Yano, Katsusuke ^e   Yabuta, Keijiro ^f   Haneda, Noriyuki ^g   Nakano, Osami ^h   Shibata, Akira ⁱ   Sawayama, Toshitami ^j   Kasai, Hideaki ^k   Yazaki, Yoshio ^l   Nakamura, Yusuke ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b GUNMA UNIVERSITY   (Japan)

^c YAMAGATA UNIVERSITY   (Japan)

^d KANAZAWA UNIVERSITY   (Japan)

^e NAGASAKI UNIVERSITY   (Japan)

^f JUNTENDO UNIVERSITY   (Japan)

^g SHIMANE UNIVERSITY   (Japan)

^h Takamatsu National Hospital   (Japan)

ⁱ NIIGATA UNIVERSITY   (Japan)

^j KAWASAKI MEDICAL SCHOOL   (Japan)

^k Tokyo Metropolitan Kiyose Children's Hospital   (Japan)

^l UNIVERSITY OF TOKYO   (Japan)

more..

Author keywords

death, sudden; genes; genetics; intervals; tachyarrhythmia; torsade de pointes

Indexed keywords

ALLELE; ARTICLE; FAMILY STUDY; GENE AMPLIFICATION; GENE MUTATION; HIGH RISK POPULATION; HUMAN; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MISSENSE MUTATION; PATHOGENESIS; PRIORITY JOURNAL; SCREENING;

EID: 16944362512     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.95.3.565     Document Type: Article

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