Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (I TO,f), are not a frequent cause of long QT syndrome

Clinica Chimica Acta

Volumn 351, Issue 1-2, 2005, Pages 95-100

  Frank Hansen, Rune ^a,b   Larsen, Lars Allan ^b,c   Andersen, Paal ^a,b   Jespersgaard, Cathrine ^a   Christiansen, Michael ^a,b  

^a STATENS SERUM INSTITUT   (Denmark)

^b Denmark   (Denmark)

^c UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

Cardiac fast transient outward current; KCND2; KCND3; Long QT syndrome; Sudden death

Indexed keywords

ION CHANNEL;

ACTION POTENTIAL; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; EXON; GENE MUTATION; GENETIC CODE; GENETIC SCREENING; HEART ELECTROPHYSIOLOGY; HEART MUSCLE; HEART MUSCLE FIBER MEMBRANE POTENTIAL; HUMAN; INTRON; LONG QT SYNDROME; MEMBRANE CURRENT; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SINGLE STRAND CONFORMATION POLYMORPHISM;

ACTION POTENTIALS; ALLELES; ANIMALS; EXONS; GENE FREQUENCY; HEART; HUMANS; INTRONS; LONG QT SYNDROME; MICE; MUTATION; MYOCARDIUM; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; POTASSIUM CHANNELS, VOLTAGE-GATED; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SHAL POTASSIUM CHANNELS;

MURINAE;

EID: 9444248630     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cccn.2004.08.017     Document Type: Article

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