(Q38290368)
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Two mutations in the promoter region of the human protein C gene both cause type I protein C deficiency by disruption of two HNF-3 binding sites (English)
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Spek CA
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Greengard JS
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Griffin JH
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Bertina RM
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Reitsma PH
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1 October 1995
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24216-24221
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Identifiers
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