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MeSH:(von Willebrand Disease/blood/*diagnosis/genetics)

1.A Case of Type 2N von Willebrand Disease with Homozygous R816W Mutation of the VWF Gene in a Nepalese Woman.

Sook Young LEE ; Eun Mi NAM ; Soon Nam LEE ; Hee Jin KIM ; Ki Sook HONG

The Korean Journal of Laboratory Medicine 2008;28(4):258-261

2.Investigation of von Willebrand Factor Gene Mutations in Korean von Willebrand Disease Patients.

Jaewoo SONG ; Jong Rak CHOI ; Kyung Soon SONG

The Korean Journal of Laboratory Medicine 2007;27(3):169-176

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