Article
Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutation.
Hematology (Amsterdam, Netherlands) - 1 Jul 2017
Su Kankan, Jin Yanhui, Miao Zhihai, Cheng Xiaoli, Yang Lihong, Wang Mingshan
Abstract excerpt
OBJECTIVE: We study the phenotype and genotype of a novel gene mutation of factor II (FII) that leads to dysprothrombinemia, and do the meta-analysis to illuminate its molecular pathogenesis. It will further contribute to our comprehension of the pathogenesis of this type of disease. METHODS: The prothrombin time (PT), activated partial thromboplastin time (APTT) and the activities of other factors were...
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