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Phenotypic and genotypic characterization of four factor VII deficiency patients from central China.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Jun 2015

Liu Hui, Wang Hua-Fang, Cheng Zhi-peng, Wang Qing-yun, Hu Bei, Zeng Wei, Wu Ying-ying, Guo Tao, Tang Liang, Hu Yu

Abstract excerpt

Hereditary coagulation factor VII deficiency (FVIID) is a rare autosomal, recessive inherited hemorrhagic disorder related to a variety of mutations or polymorphisms throughout the factor VII (FVII) gene (F7). The aims of this study were to characterize the molecular defect of the F7 gene in four unrelated patients with FVIID and to find the genotype-phenotype correlation. All nine exons, exon-intron boundaries,...

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PMID: 25767893
DOI: 10.1097/MBC.0000000000000279

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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