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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English | 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)
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Naoki Mochizuki
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Dan M Roden
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Alfred L George
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Naomasa Makita
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Wataru Shimizu
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Minoru Horie
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Akihiko Sunami
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Eric Schulze-Bahr
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Shigetomo Fukuhara
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Takeru Makiyama
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Hideki Itoh
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Michael Christiansen
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Pascal McKeown
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Koji Miyamoto
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Shiro Kamakura
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Hiroyuki Tsutsui
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1 June 2008
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2219-2229
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