Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel

Circulation

Volumn 99, Issue 24, 1999, Pages 3165-3171

  Wei, Jian ^a   Wang, Dao W ^a   Alings, Marco ^c   Fish, Frank ^a   Wathen, Mark ^d   Roden, Dan M ^a   George Jr , Alfred L ^a,b  

^a VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^c NONE   (Netherlands)

^d NONE

Author keywords

Genes; Heart defects, congenital; Long QT syndrome; SCN5A; Sodium channel

Indexed keywords

SODIUM CHANNEL;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CARBOXY TERMINAL SEQUENCE; CHANNEL GATING; ELECTROPHYSIOLOGY; EXON; FAMILY; GENE MUTATION; HEART MUSCLE EXCITABILITY; HEART REPOLARIZATION; HEART VENTRICLE TACHYCARDIA; HUMAN; LONG QT SYNDROME; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SITE DIRECTED MUTAGENESIS; STRUCTURE ACTIVITY RELATION; SUDDEN DEATH; XENOPUS;

EID: 0033594970     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.99.24.3165     Document Type: Article

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