KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome

Circulation

Volumn 96, Issue 9, 1997, Pages 2778-2781

  Donger, Claire ^a   Denjoy, Isabelle ^b,c   Berthet, Myriam ^a   Neyroud, Nathalie ^a,b   Cruaud, Corinne ^d   Bennaceur, Mohammed ^a   Chivoret, Guy ^e   Schwartz, Ketty ^a   Coumel, Philippe ^b   Guicheney, Pascale ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b HÔPITAL LARIBOISIÈRE   (France)

^c Château des Côtes   (France)

^d CNRS   (France)

^e CHU NANCY BRABOIS   (France)

Author keywords

Antiarrhythmia agents; Congenital; Death, sudden; Heart defects; Tachyarrhythmias

Indexed keywords

POTASSIUM CHANNEL;

ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; ENZYME SUBUNIT; FEMALE; GENETIC LINKAGE; HUMAN; LONG QT SYNDROME; MALE; MISSENSE MUTATION; PATHOGENESIS; PRIORITY JOURNAL; SUDDEN DEATH; SYNCOPE;

EID: 19244371485     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.96.9.2778     Document Type: Article

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