Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion

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Erscheinungsjahr:
2014
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Text
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  • info:eu-repo/semantics/restrictedAccess
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Forschungsinformationssystem des UKE

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oai:pure.atira.dk:publications/ac49992a-6625-49f6-9a81-72d663c9d342