Factor VIII deficiency not induced by FVIII gene mutation in a female first cousin of two brothers with haemophilia A
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2002.03819.x/fullpdf
Reference10 articles.
1. Factor VIII gene inversions in seVere haemophilia A: results of an international consortium study;Antonarakis;Blood,1995
2. Characterization of factor VIII gene inversions using a non-radioactive detection method: a survey of 102 unrelated haemophilia A families from Northern France;Gaucher;Nouvelle Revue Française D'hématologie,1995
3. The ‘Normandy’ variant of von Willebrand disease: characterization of a point mutation in the von Willebrand factor gene;Gaucher;Blood,1991
4. The life cycle of coagulation factor VIII in view of its structure and function;Lenting;Blood,1998
5. Evidence for a von Willebrand factor defect in factor VIII binding in three members of a family previously misdiagnosed mild Haemophilia A and Haemophilia A carriers: consequences for therapy and genetic counselling;Mazurier;British Journal of Haematology,1990
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