Clinical Phenotype and Genetic Analysis of Twins With Congenital Coagulation Factor V Deficiency
Conclusion:
In this set of twins, missense mutations of the FV gene were related to congenital FV deficiency but unrelated to the patent foramen ovale observed in the older boy.
Source: Journal of Pediatric Hematology Oncology - Category: Hematology Tags: Online Articles: Clinical and Laboratory Observations Source Type: research
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