- A Case of Type 2N von Willebrand Disease with Homozygous R816W Mutation of the VWF Gene in a Nepalese Woman
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Lee SY, Nam EM, Lee SN, Kim HJ, Hong KS
- KMID: 854886
- Korean J Lab Med.
- 2008 Aug;28(4):258-261.
- doi: 10.3343/kjlm.2008.28.4.258
Type 2N von Willebrand disease (vWD) can be confused with hemophilia A due to decreased factor VIII levels and a bleeding tendency, and differential diagnosis is of importance for providing... -
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