A single Na+ channel mutation causing both long-QT and Brugada syndromes

Circulation Research

Volumn 85, Issue 12, 1999, Pages 1206-1213

  Bezzina, Connie ^a   Veldkamp, Marieke W ^a   Van Den Berg, Maarten P ^b   Postma, Alex V ^a   Rook, Martin B ^c   Viersma, Jan Willem ^b   Van Langen, Irene M ^a   Tan Sindhunata, Ghita ^b   Bink Boelkens, Margreet Th E ^b   Van Der Hout, Annemarie H ^b   Mannens, Marcel M A M ^a   Wilde, Arthur A M ^a,c  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

Arrhythmia; Brugada syndrome; Long QT syndrome; Na+ channel; SCN5A

Indexed keywords

PROCAINAMIDE; SODIUM CHANNEL;

ADULT; ARTICLE; BRUGADA SYNDROME; CONTROLLED STUDY; FEMALE; GENE EXPRESSION SYSTEM; GENETIC LINKAGE; HETEROZYGOTE; HUMAN; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MALE; MUTATION; PEDIGREE; PHENOTYPE; PR INTERVAL; PRIORITY JOURNAL; QRS COMPLEX; QT INTERVAL; ST SEGMENT ELEVATION; SUDDEN DEATH; XENOPUS;

XENOPUS;

EID: 0033533990     PISSN: 00097330     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.RES.85.12.1206     Document Type: Article

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