Loss-of-function mutations of the K(+) channel gene KCNJ2 constitute a rare cause of long QT syndrome (Q44994275)
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Language | Label | Description | Also known as |
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English | Loss-of-function mutations of the K(+) channel gene KCNJ2 constitute a rare cause of long QT syndrome |
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Loss-of-function mutations of the K(+) channel gene KCNJ2 constitute a rare cause of long QT syndrome (English)
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Heidi Fodstad
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Heikki Swan
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Muriel Auberson
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Ivan Gautschi
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Johannes Loffing
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Laurent Schild
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Kimmo Kontula
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1 August 2004
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37
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2
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593-602
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