Mutation of the gene for IsK associated with both Jervell and Lange- Nielsen and Romano-Ward forms of long-QT syndrome

Circulation

Volumn 97, Issue 2, 1998, Pages 142-146

  Duggal, Priya ^a   Vesely, Mark R ^a   Wattanasirichaigoon, Duangrurdee ^a   Villafane, Juan ^b   Kaushik, Vineet ^c   Beggs, Alan H ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b University of Louisville School of Medicine   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

Author keywords

Arrhythmia; Genes; Long QT syndrome; Molecular biology; Syncope

Indexed keywords

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; FEMALE; GENE LOCUS; GENE MUTATION; HUMAN; LONG QT SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; QT INTERVAL; SCHOOL CHILD;

EID: 0031936234     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.97.2.142     Document Type: Article

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