HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects

Journal of Biological Chemistry

Volumn 273, Issue 33, 1998, Pages 21061-21066

  Zhou, Zhengfeng ^a   Gong, Qiuming ^a   Epstein, Miles L ^b   January, Craig T ^a,c  

^a UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

^c University of Wisconsin Health   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL;

ARTICLE; CHANNEL GATING; HUMAN; LONG QT SYNDROME; MOLECULAR CLONING; PATHOGENESIS; PRIORITY JOURNAL; SITE DIRECTED MUTAGENESIS;

BIOLOGICAL TRANSPORT; BLOTTING, WESTERN; CATION TRANSPORT PROTEINS; CELL LINE; DNA-BINDING PROTEINS; ETHER-A-GO-GO POTASSIUM CHANNELS; HUMANS; LONG QT SYNDROME; MUTAGENESIS, SITE-DIRECTED; PATCH-CLAMP TECHNIQUES; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED; PROTEIN PROCESSING, POST-TRANSLATIONAL; TRANS-ACTIVATORS; TRANSFECTION;

EID: 0032516934     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.273.33.21061     Document Type: Article

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