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About this Medicine article
N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome by Ohno, Seiko; Zankov, Dimitar P.; Yoshida, Hidetada; Tsuji, Keiko; Makiyama, Takeru; Itoh, Hideki; Akao, Masaharu; Hancox, Jules C.; Kita, Toru; Horie, Minoru is a Medicine article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Medicine.
- Author
- Ohno, Seiko; Zankov, Dimitar P.; Yoshida, Hidetada; Tsuji, Keiko; Makiyama, Takeru; Itoh, Hideki; Akao, Masaharu; Hancox, Jules C.; Kita, Toru; Horie, Minoru
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 1547-5271)
- Published
- 2007
- Language
- EN
- Field
- Medicine (Health Sciences)