N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome

Heart Rhythm

Volumn 4, Issue 3, 2007, Pages 332-340

  Ohno, Seiko ^a   Zankov, Dimitar P ^b   Yoshida, Hidetada ^a   Tsuji, Keiko ^b   Makiyama, Takeru ^a   Itoh, Hideki ^b   Akao, Masaharu ^a   Hancox, Jules C ^c   Kita, Toru ^a   Horie, Minoru ^b  

^a KYOTO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

^c UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

Electrophysiology; Ion channels; KCNE1; Long QT syndrome; Molecular screening

Indexed keywords

ADAPTOR PROTEIN; ION CHANNEL; POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNE1; POTASSIUM CHANNEL KCNQ1; UNCLASSIFIED DRUG;

ADULT; AGED; AMINO TERMINAL SEQUENCE; ARTICLE; ARTIFICIAL HEART PACEMAKER; BRADYCARDIA; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ELECTROCARDIOGRAPHY; EXERCISE; FEMALE; GENE EXPRESSION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; HEART ELECTROPHYSIOLOGY; HEART PALPITATION; HUMAN; HUMAN CELL; INHERITANCE; JAPANESE; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PHENOTYPE; POTASSIUM CURRENT; PRIORITY JOURNAL; PROTEIN DOMAIN; QT PROLONGATION; REST; SEQUENCE ANALYSIS; SITE DIRECTED MUTAGENESIS; SYMPTOM; SYNCOPE;

ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; ELECTROCARDIOGRAPHY; ELECTROPHYSIOLOGIC TECHNIQUES, CARDIAC; ETHER-A-GO-GO POTASSIUM CHANNELS; FEMALE; GENE EXPRESSION; GENETIC SCREENING; GENOTYPE; HUMANS; JAPAN; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; MUTATION, MISSENSE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; POTASSIUM CHANNELS, VOLTAGE-GATED; RESEARCH DESIGN;

EID: 33847284166     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2006.11.004     Document Type: Article

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