Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias

Human Molecular Genetics

Volumn 6, Issue 11, 1997, Pages 1943-1949

  Wollnik, Bernd ^a   Schroeder, Björn C ^a   Kubisch, Christian ^a   Esperer, Hans D ^b   Wieacker, Peter ^b   Jentsch, Thomas J ^a  

^a UNIVERSITY OF HAMBURG   (Germany)

^b OTTO VON GUERICKE UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MUTANT PROTEIN; POTASSIUM CHANNEL; POTASSIUM ION;

ALTERNATIVE RNA SPLICING; AMINO ACID SUBSTITUTION; ARTICLE; CARBOXY TERMINAL SEQUENCE; CLINICAL ARTICLE; DELETION MUTANT; DOMINANT INHERITANCE; GENE EXPRESSION; GENE MUTATION; HEART ARRHYTHMIA; HUMAN; HUMAN CELL; LONG QT SYNDROME; PATHOPHYSIOLOGY; POTASSIUM CURRENT; PRIORITY JOURNAL; PROTEIN VARIANT; TRANSPORT KINETICS;

AMINO ACID SEQUENCE; BASE SEQUENCE; CLONING, MOLECULAR; DNA, COMPLEMENTARY; FEMALE; GENES, DOMINANT; GENES, RECESSIVE; HUMANS; KCNQ POTASSIUM CHANNELS; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED;

EID: 0030782276     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.11.1943     Document Type: Article

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