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A large deletion identified in a Swedish family with type 1 VWD.

Anna M Johansson, Elsa Lanke, Torbjörn Säll, Stefan Lethagen, Christer Halldén

Thrombosis and haemostasis 2011 Apr


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  • family (2)
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  • humans (1)
  • microsatellite repeats (1)
  • pedigree (1)
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  • polymorphism single nucleotide (1)
  • sequence deletion (1)
  • sweden (1)
  • von willebrand disease (1)
  • von willebrand disease, type 1 (2)
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    No abstract available.

    Citation

    Anna M Johansson, Elsa Lanke, Torbjörn Säll, Stefan Lethagen, Christer Halldén. A large deletion identified in a Swedish family with type 1 VWD. Thrombosis and haemostasis. 2011 Apr;105(4):733-4

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    PMID: 21225094

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