Molecular analysis of the prothrombin gene in two patients

A deficiency of prothrombin (Fil) is an extremely rare bleeding disorder. Two patients were studied with a severe form of this disorder which is known as Hypoprothrombinemia. Each patient was identified as being the product of a consanguineous union, and therefore a single homozygous mutation wo...

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Bibliographic Details
Main Author: Duke, Leslea Marie
Language:English
Published: 2009
Online Access:http://hdl.handle.net/2429/4983

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