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A case of long QT syndrome with triple gene abnormalities: Digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1

✍ Scribed by Yoshikane, Yukako; Yoshinaga, Masao; Hamamoto, Kunihiro; Hirose, Shinichi

Book ID: 120440373
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 521 KB
Volume: 10
Category: Article
ISSN: 1547-5271
DOI: 10.1016/j.hrthm.2012.12.008

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