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Volumn 105, Issue 7, 2002, Pages 794-799
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Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel
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Author keywords
Arrhythmia; Genes; Long QT syndrome
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Indexed keywords
POTASSIUM CHANNEL;
POTASSIUM CHANNEL HERG;
ADOLESCENT;
ADULT;
ARTICLE;
CARDIOVASCULAR RISK;
CLINICAL FEATURE;
CONTROLLED STUDY;
DISEASE COURSE;
FEMALE;
GENE;
GENE LOCATION;
GENE MUTATION;
HEART ARRHYTHMIA;
HUMAN;
LONG QT SYNDROME;
MAJOR CLINICAL STUDY;
MALE;
PRIORITY JOURNAL;
PROGNOSIS;
REGRESSION ANALYSIS;
ADOLESCENT;
ADULT;
ARRHYTHMIA;
BINDING SITES;
CATION TRANSPORT PROTEINS;
DISEASE PROGRESSION;
DNA MUTATIONAL ANALYSIS;
DNA-BINDING PROTEINS;
ELECTROCARDIOGRAPHY;
ETHER-A-GO-GO POTASSIUM CHANNELS;
FEMALE;
FOLLOW-UP STUDIES;
HUMANS;
LONG QT SYNDROME;
MALE;
MODELS, MOLECULAR;
MUTATION;
ODDS RATIO;
PHENOTYPE;
POTASSIUM CHANNELS;
POTASSIUM CHANNELS, VOLTAGE-GATED;
PROGNOSIS;
PROPORTIONAL HAZARDS MODELS;
REGISTRIES;
REGRESSION ANALYSIS;
RISK ASSESSMENT;
SURVIVAL ANALYSIS;
TRANS-ACTIVATORS;
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EID: 0037133307
PISSN: 00097322
EISSN: None
Source Type: Journal
DOI: 10.1161/hc0702.105124 Document Type: Article |
Times cited : (346)
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References (22)
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