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Identification and characterization of a novel genetic mutation with prolonged QT syndrome in an unexplained postoperative death

✍ Scribed by Yukiko Hata, Hisashi Mori, Ayumi Tanaka…

Book ID: 120897671
Publisher: Springer-Verlag
Year: 2013
Tongue: German
Weight: 847 KB
Volume: 128
Category: Article
ISSN: 0937-9827
DOI: 10.1007/s00414-013-0853-4

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Long QT (LQT) syndrome is a potentially life-threatening disorder, characterized by a distinct cardiac arrhythmia known as torsades de pointes. Mutations within a number of genes linked to the familial form, including that coding for a cardiac potassium channel called KCNH2 (HERG), have been describ