(Q32007490)
Statements
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Molecular mechanism of type I congenital heparin cofactor (HC) II deficiency caused by a missense mutation at reactive P2 site: HC II Tokushima (English)
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Kanagawa Y
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Shigekiyo T
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Aihara K
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Akaike M
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Azuma H
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Matsumoto T
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1 January 2001
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101-107
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Identifiers
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