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

✍ Scribed by Wei Li; Qiu-fen Wang; Rong Du; Qiu-Mei Xu; Qin-Mei Ke; Bin Wang; Xue-Lin Chen; Li Tian; Shou-Yan Zhang; Cai-Lian Kang; Si-Ming Guan; Jun-Guo Yang; Zi-Fang Song

Book ID: 116298081
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 657 KB
Volume: 380
Category: Article
ISSN: 0006-291X
DOI: 10.1016/j.bbrc.2009.01.051

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