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Article

Coagulation factor XI: a database of mutations and polymorphisms associated with factor XI deficiency.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Jun 2005

Dossenbach-Glaninger Astrid, Hopmeier Pierre

Abstract excerpt

Hereditary factor XI deficiency is a rare bleeding disorder that is found worldwide. Rapidly increasing numbers of mutations and polymorphisms in various populations have been reported. However, the number of identified mutations given in recent literature and available databases is named to be not more than 35. We assumed that this is clearly too low and that to date no comprehensive survey of mutations...

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PMID: 15870541
DOI: 10.1097/01.mbc.0000169214.62560.a5

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