(Q33335804)
Statements
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Missense C168T in the Wiskott--Aldrich Syndrome protein gene is a common mutation in X-linked thrombocytopenia (English)
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Ho LL
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Ayling J
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Prosser I
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Kronenberg H
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Iland H
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Joshua D
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1 January 2001
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112
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76-80
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Identifiers
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