Spectrum of mutations in Long-QT Syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

Circulation

Volumn 102, Issue 10, 2000, Pages 1178-1185

  Splawski, Igor ^a   Shen, Jiaxiang ^b   Timothy, Katherine W ^a   Lehmann, Michael H ^e   Priori, Silvia ^f   Robinson, Jennifer L ^h   Moss, Arthur J ^h   Schwartz, Peter J ^g   Towbin, Jeffrey A ⁱ   Vincent, G Michael ^d   Keating, Mark T ^a,b,c  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^c UNIVERSITY OF UTAH   (United States)

^d LDS HOSPITAL   (United States)

^e UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^f IRCCS   (Italy)

^g FONDAZIONE IRCCS POLICLINICO SAN MATTEO   (Italy)

^h UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

ⁱ BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Arrhythmia; Death, sudden; Genetics; Long QT syndrome; Torsade de pointes

Indexed keywords

ADULT; AGED; ARTICLE; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE MUTATION; HUMAN; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NONSENSE MUTATION; PRIORITY JOURNAL;

EID: 0034609531     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.102.10.1178     Document Type: Article

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