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Article

Genotypes and phenotypes characterization of 17 Iranian patients with inherited factor X deficiency: identification of a novel mutation: Leu487Phe.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Mar 2022

Fallah Aysan, Shams Mahmood, Agi Elnaz, Jazebi Mohammad, Baghaipoor Mohammad R, Naderi Tohid, Rezvany Mohammad R

Abstract excerpt

Factor X deficiency is a rare bleeding disorder that affects almost 1 : 1000 000 people worldwide. It derives from multiple mutational changes in the factor X gene (F10). The main objective of the present study was to determine a consistent correlation between the clinical presentations and causative genotype. The phenotype and genotype of 17 Iranian patients with reduced factor X activity (FX:C) from 14...

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PMID: 35140190
DOI: 10.1097/MBC.0000000000001101

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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