Dysfunctional potassium channel subunit interaction as a novel mechanism of long QT syndrome

Heart Rhythm

Volumn 10, Issue 5, 2013, Pages 728-737

  Hoosien, Michael ^a   Ellen Ahearn, Mary ^a   Myerburg, Robert J ^a   Pham, Thai V ^a   Miller, Todd E ^a   Smets, Marcel J ^a   Baumbach Reardon, Lisa ^a   Young, Ming Lon ^a   Farooq, Amjad ^a   Bishopric, Nanette H ^a  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

Arrhythmia; Genetics; Ion channels; Long QT syndrome; Structural modeling

Indexed keywords

MYC PROTEIN; POTASSIUM CHANNEL KCNE1;

ANIMAL CELL; ARTICLE; BRADYCARDIA; COMPUTER PROGRAM; CONTROLLED STUDY; DISEASE COURSE; EPITOPE MAPPING; FEMALE; GENE MUTATION; HUMAN; HUMAN CELL; IMMUNOHISTOCHEMISTRY; LONG QT SYNDROME; NONHUMAN; POTASSIUM CURRENT; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN EXPRESSION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; QT INTERVAL; TORSADE DES POINTES;

ANIMALS; CHILD; ELECTROCARDIOGRAPHY; HUMANS; INFANT, NEWBORN; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; MALE; MUTATION; PEDIGREE; POTASSIUM CHANNELS, VOLTAGE-GATED; XENOPUS;

EID: 84876550604     PISSN: 15475271     EISSN: 15563871     Source Type: Journal    
DOI: 10.1016/j.hrthm.2012.12.033     Document Type: Article

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