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3. Identification of two novel missense mutations causing severe factor XIII deficiency. Handrkova H; Borhany M; Schroeder V; Fatima N; Hussain A; Shamsi T; Kohler HP Haemophilia; 2015 May; 21(3):e253-e256. PubMed ID: 25832324 [No Abstract] [Full Text] [Related]
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9. Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations. Katona É; Muszbek L; Devreese K; Kovács KB; Bereczky Z; Jonkers M; Shemirani AH; Mondelaers V; Ermens AA Haemophilia; 2014 Jan; 20(1):114-20. PubMed ID: 24118344 [TBL] [Abstract][Full Text] [Related]
10. First trimester prenatal diagnosis of severe FXIII deficiency. Shanbhag S; Ghosh K; Shetty S Haemophilia; 2016 Sep; 22(5):e443-4. PubMed ID: 27340806 [No Abstract] [Full Text] [Related]
11. 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. Souri M; Biswas A; Misawa M; Omura H; Ichinose A Haemophilia; 2014 Mar; 20(2):255-62. PubMed ID: 24286209 [TBL] [Abstract][Full Text] [Related]
12. Biology of Factor XIII and clinical manifestations of Factor XIII deficiency. Levy JH; Greenberg C Transfusion; 2013 May; 53(5):1120-31. PubMed ID: 22928875 [TBL] [Abstract][Full Text] [Related]
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