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Congenital long QT syndrome with compound mutations in the KCNH2 gene

✍ Scribed by Bando, Sachiko; Soeki, Takeshi; Matsuura, Tomomi; Niki, Toshiyuki; Ise, Takayuki; Yamaguchi, Koji; Taketani, Yoshio; Iwase, Takashi; Yamada, Hirotsugu; Wakatsuki, Tetsuzo; Akaike, Masashi; Aiba, Takeshi; Shimizu, Wataru; Sata, Masataka

Book ID: 125345701
Publisher: Springer
Year: 2013
Tongue: English
Weight: 613 KB
Volume: 29
Category: Article
ISSN: 0910-8327
DOI: 10.1007/s00380-013-0406-2

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