Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndrome

Journal of Molecular and Cellular Cardiology

Volumn 28, Issue 9, 1996, Pages 2051-2055

  Tesson, Frédérique ^a   Donger, Claire ^a   Denjoy, Isabelle ^b   Berthet, Myriam ^a   Bennaceur, Mohammed ^a   Petit, Christine ^c   Coumel, Philippe ^b   Schwartz, Ketty ^a   Guicheney, Pascale ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b HÔPITAL LARIBOISIÈRE   (France)

^c INSTITUT PASTEUR   (France)

Author keywords

IsK; Jervell and Lange Nielsen syndrome; KCNE1; Long QT syndrome; Potassium channel; RFLP

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT; MEMBRANE PROTEIN; POTASSIUM CHANNEL;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 21; CLINICAL ARTICLE; CONSANGUINITY; DNA POLYMORPHISM; FEMALE; GENETIC ANALYSIS; GENETIC LINKAGE; HEARING IMPAIRMENT; HEART REPOLARIZATION; HEART VENTRICLE; HUMAN; LONG QT SYNDROME; MALE; MARKER GENE; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; PROTEIN DOMAIN; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE STRAND CONFORMATION POLYMORPHISM; SUDDEN DEATH; SYNCOPE;

EID: 0030248659     PISSN: 00222828     EISSN: None     Source Type: Journal    
DOI: 10.1006/jmcc.1996.0198     Document Type: Article

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