1. 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. (29th November 2013) Authors: Souri, M.; Biswas, A.; Misawa, M.; Omura, H.; Ichinose, A. Journal: Haemophilia Issue: Volume 20:Number 2(2014:Mar.) Page Start: 255 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 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. (29th November 2013) Authors: Souri, M.; Biswas, A.; Misawa, M.; Omura, H.; Ichinose, A. Journal: Haemophilia Issue: Volume 20:Number 2(2014:Mar.) Page Start: 255 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗