Factor VIII deficiency not induced by FVIII gene mutation in a female first cousin of two brothers with haemophilia A.

Article Details

Citation

Mazurier C, Parquet-Gernez A, Gaucher C, Lavergne JM, Goudemand J

Factor VIII deficiency not induced by FVIII gene mutation in a female first cousin of two brothers with haemophilia A.

Br J Haematol. 2002 Nov;119(2):390-2.

PubMed ID
12406074 [ View in PubMed
]
Abstract

In this study, we reinvestigated a 20-year-old woman, the first cousin of two brothers with severe haemophilia A. This patient was previously assumed to be a carrier of haemophilia A due to her FVIII deficiency. We identified a novel FVIII gene mutation in the family and demonstrated that the FVIII deficiency in this female patient did not result from this gene mutation, but was linked to molecular defects in the von Willebrand factor gene.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Coagulation factor VIIIP00451Details
von Willebrand factorP04275Details