A mutation in HERG associated with notched T waves in long QT syndrome

Journal of Molecular and Cellular Cardiology

Volumn 28, Issue 8, 1996, Pages 1609-1615

  Dausse, Eric ^a   Berthet, Myriam ^a   Denjoy, Isabelle ^b   André Fouet, Xavier ^c   Cruaud, Corrine ^d   Bennaceur, Mohammed ^e   Fauré, Sabine ^d   Coumel, Philippe ^b   Schwartz, Ketty ^a   Guicheney, Pascale ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b HÔPITAL LARIBOISIÈRE   (France)

^c LOUIS PRADEL HOSPITAL   (France)

^d CNRS   (France)

^e NONE

Author keywords

Chromosome 7; HERG; Long QT syndrome; Potassium channel; T wave morphology

Indexed keywords

ALANINE; POTASSIUM CHANNEL; THREONINE;

ARTICLE; CHROMOSOME 11; CHROMOSOME 3; CHROMOSOME 4; CHROMOSOME 7; CLINICAL ARTICLE; CODON; ELECTROCARDIOGRAPHY; FEMALE; GENE LOCUS; GENE MUTATION; HEART ARRHYTHMIA; HUMAN; LONG QT SYNDROME; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SUDDEN DEATH; T WAVE;

EID: 0030218890     PISSN: 00222828     EISSN: None     Source Type: Journal    
DOI: 10.1006/jmcc.1996.0151     Document Type: Article

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