The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome (Q36597505)

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scientific article published on June 2008
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The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
scientific article published on June 2008

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    The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome (English)
    Naomasa Makita
    Wataru Shimizu
    Minoru Horie
    Akihiko Sunami
    Eric Schulze-Bahr
    Shigetomo Fukuhara
    Takeru Makiyama
    Hideki Itoh
    Michael Christiansen
    Pascal McKeown
    Koji Miyamoto
    Shiro Kamakura
    Hiroyuki Tsutsui
    Alfred L George
    1 June 2008
    118
    2219-2229

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