Ion channel mechanisms related to sudden cardiac death in phenotype-negative long-QT syndrome genotype-phenotype correlations of the KCNQ1(S349W) mutation

Journal of Cardiovascular Electrophysiology

Volumn 22, Issue 2, 2011, Pages 193-200

  Horr, Samuel ^a   Goldenberg, Ilan ^b   Moss, Arthur J ^a   O Uchi, Jin ^a   Barsheshet, Alon ^a   Connelly, Heather ^a   Gray, Daniel A ^a   Zareba, Wojciech ^a   Lopes, Coeli M B ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^b University of Rochester Medical Center ^*

Author keywords

corrected QT interval; long QT syndrome; potassium ion channel current; sudden death; ventricular tachycardia

Indexed keywords

POTASSIUM CHANNEL KCNQ1;

ADULT; ANIMAL CELL; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOTE; HUMAN; ION CONDUCTANCE; ION CURRENT; LONG QT SYNDROME; MALE; MISSENSE MUTATION; NONHUMAN; NONSENSE MUTATION; OUTCOME ASSESSMENT; PRIORITY JOURNAL; QT PROLONGATION; SUDDEN DEATH; WILD TYPE;

CHILD; DEATH, SUDDEN, CARDIAC; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; ION CHANNEL GATING; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; MALE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 79951653454     PISSN: 10453873     EISSN: 15408167     Source Type: Journal    
DOI: 10.1111/j.1540-8167.2010.01852.x     Document Type: Article

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