APA (7th ed.) Citation

T, O., M, S., YS, S., N, I., R, L., & A, I. (2016). Molecular pathogenesis of plasminogen Hakodate: The second Japanese family case of severe type I plasminogen deficiency manifested late-onset multi-organic chronic pseudomembranous mucositis. Journal of thrombosis and thrombolysis, 42(2), 218. https://doi.org/10.1007/s11239-016-1375-y

Chicago Style (17th ed.) Citation

T, Osaki, Souri M, Song YS, Izumi N, Law R, and Ichinose A. "Molecular Pathogenesis of Plasminogen Hakodate: The Second Japanese Family Case of Severe Type I Plasminogen Deficiency Manifested Late-onset Multi-organic Chronic Pseudomembranous Mucositis." Journal of Thrombosis and Thrombolysis 42, no. 2 (2016): 218. https://doi.org/10.1007/s11239-016-1375-y.

MLA (9th ed.) Citation

T, Osaki, et al. "Molecular Pathogenesis of Plasminogen Hakodate: The Second Japanese Family Case of Severe Type I Plasminogen Deficiency Manifested Late-onset Multi-organic Chronic Pseudomembranous Mucositis." Journal of Thrombosis and Thrombolysis, vol. 42, no. 2, 2016, p. 218, https://doi.org/10.1007/s11239-016-1375-y.