Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block

Circulation

Volumn 105, Issue 3, 2002, Pages 341-346

  Wang, Dao W ^a   Viswanathan, Prakash C ^a   Balser, Jeffrey R ^a   George Jr , Alfred L ^a   Benson, D Woodrow ^a  

^a CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

Arrhythmia; Bundle branch block; Genetics; Long QT syndrome

Indexed keywords

ION CHANNEL; SODIUM CHANNEL;

ACTION POTENTIAL; ADULT; AGED; ALPHA CHAIN; AMINO ACID SUBSTITUTION; ARTICLE; ATRIOVENTRICULAR BLOCK; BIOPHYSICS; BRUGADA SYNDROME; CELL CULTURE; CHILD; CLINICAL ARTICLE; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HEART ARRHYTHMIA; HEART BUNDLE BRANCH BLOCK; HEART MUSCLE CONDUCTION SYSTEM; HETEROZYGOSITY; HUMAN; HUMAN CELL; LONG QT SYNDROME; MALE; MOLECULAR GENETICS; NERVE CONDUCTION; NUCLEIC ACID BASE SUBSTITUTION; PATCH CLAMP; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; SODIUM CURRENT;

ACTION POTENTIALS; ADULT; AMINO ACID SEQUENCE; ATRIOVENTRICULAR NODE; CELL LINE; CHILD; COMPUTER SIMULATION; ELECTROCARDIOGRAPHY; FEMALE; HEART BLOCK; HUMANS; KINETICS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PATCH-CLAMP TECHNIQUES; PROTEIN STRUCTURE, TERTIARY; SEQUENCE HOMOLOGY, AMINO ACID; SODIUM CHANNELS;

EID: 0037154288     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/hc0302.102592     Document Type: Article

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