A family with type 2M VWD with normal VWF:RCo but reduced VWF:CB and a M1761K mutation in the A3 domain.

作者: D. KEELING , J. BEAVIS , R. MARR , K. SUKHU , P. BIGNELL

DOI: 10.1111/J.1365-2516.2011.02676.X

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参考文章(6)
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