(Q24629583)

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Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease

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Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease (English)
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H Kasahara
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B Lee
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J J Schott
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D W Benson
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C E Seidman
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S Izumo
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July 2000
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106
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2
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299-308
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