Congenital long QT syndrome caused by the F275S KCNQ1 mutation: Mechanism of impaired channel function

Biochemical and Biophysical Research Communications

Volumn 380, Issue 1, 2009, Pages 127-131

  Li, Wei ^a   Wang, Qiu fen ^a   Du, Rong ^a   Xu, Qiu Mei ^a   Ke, Qin Mei ^a   Wang, Bin ^a   Chen, Xue Lin ^a   Tian, Li ^a   Zhang, Shou Yan ^a   Kang, Cai Lian ^a   Guan, Si Ming ^a   Yang, Jun Guo ^a   Song, Zi Fang ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

ER retention; KCNQ1; Long QT syndrome; Trafficking

Indexed keywords

POTASSIUM CHANNEL KCNQ1;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; ENZYME ACTIVATION; FEMALE; HUMAN; HUMAN CELL; LONG QT SYNDROME; MISSENSE MUTATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION;

ANIMALS; CELL LINE; ENDOPLASMIC RETICULUM; HUMANS; KCNQ1 POTASSIUM CHANNEL; LONG QT SYNDROME; MUTATION, MISSENSE; PHENYLALANINE; PROTEIN TRANSPORT; SERINE;

EID: 59649096971     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.01.051     Document Type: Article

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