Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation

Journal of Biological Chemistry

Volumn 274, Issue 15, 1999, Pages 10113-10118

  Chen, Jun ^a   Zou, Anrou ^a   Splawski, Igor ^b,c   Keating, Mark T ^a,b,c   Sanguinetti, Michael C ^a,c  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^c UNIVERSITY OF UTAH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; GENE EXPRESSION; GENE MUTATION; HEART MUSCLE POTENTIAL; HEART REPOLARIZATION; LONG QT SYNDROME; NONHUMAN; OOCYTE; PATHOGENESIS; POTASSIUM CURRENT; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN PROTEIN INTERACTION; QT INTERVAL; VOLTAGE CLAMP; XENOPUS;

ANIMALIA;

EID: 0033537885     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.274.15.10113     Document Type: Article

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