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APA Citation
Souri, M., Biswas, A., Misawa, M., Omura, H., & Ichinose, A. (n.d.). severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines. Haemophilia, 20, 255–262. http://access.bl.uk/ark:/81055/vdc_100024787420.0x00003a