Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome (Q57807317)

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Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome
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    Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome (English)
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    L A Larsen
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    P S Andersen
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    J Kanters
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    I H Svendsen
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    J R Jacobsen
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    J Vuust
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    G Wettrell
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    L Tranebjaerg
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    J Bathen
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    M Christiansen
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    August 2001
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    47
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    8
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    1390-5
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