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...
| Main Author: | |
|---|---|
| Language: | English |
| Published: |
2009
|
| Online Access: | http://hdl.handle.net/2429/4983 |
Search Result 1
