bibliographicCitation |
Shigekiyo T, Yagi H, Sekimoto E, Shibata H, Ozaki S, Matsumoto M. Identification of a missense mutation (p.Leu1733Pro) in the A3 domain of von Willebrand factor in a family with type 2M von Willebrand disease. International Journal of Hematology. 2019 Oct 11;111(3):467–70. doi: 10.1007/s12185-019-02753-4. |