Characterization of a novel, dominant negative KCNJ2 mutation associated with Andersen-Tawil syndrome

Channels

Volumn 5, Issue 6, 2011, Pages 500-509

  Marrus, Scott B ^a   Cuculich, Phillip S ^a   Wang, Wei ^a   Nerbonne, Jeanne M ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Andersen Tawil syndrome; Inward rectifier; Ion channels; K channel; Kir2.1

Indexed keywords

INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR2.1; ION CHANNEL;

ADULT; AMINO ACID SUBSTITUTION; ANDERSEN SYNDROME; ANIMAL CELL; ARTICLE; CASE REPORT; ELECTROCARDIOGRAM; GENE MUTATION; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENETIC TRANSFECTION; HEART EXCITATION; HEART MUSCLE CELL; HEART MUSCLE EXCITABILITY; HEART MUSCLE POTENTIAL; HEART VENTRICLE BIGEMINY; HUMAN; HUMAN CELL; KINETICS; MALE; MOUSE; MUSCLE WEAKNESS; NONHUMAN; PROTEIN EXPRESSION; SIMULATION; SYNDACTYLY; VOLTAGE CLAMP;

EID: 84455182949     PISSN: 19336950     EISSN: 19336969     Source Type: Journal    
DOI: 10.4161/chan.5.6.18524     Document Type: Article

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