Case Report: Novel Mutation of F5 With Maternal Uniparental Disomy Causes Severe Congenital Factor V Deficiency

Overview of attention for article published in Frontiers in Pediatrics, June 2022

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New Research: Case Report: Novel Mutation of F5 With Maternal Uniparental Disomy Causes Severe Congenital Factor V Deficiency: We summarized two cases of congenital factor V deficiency (FVD) associated with a novel F5 mutation, and analyzed… https://t.co/M

13 Jul 2022

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