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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| Language: | English |
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2009
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| Online Access: | http://hdl.handle.net/2429/4983 |