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The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia A.

Archives of Iranian medicine - 1 Dec 2021

Azadmehr Sarah, Rahiminejad Faezeh, Zafarghandi Motlagh Fatemeh, Jamali Mojdeh, Ghazizadeh Tehrani Pardis, Shirzadeh Tina, Bagherian Hamideh, Karimipoor Morteza, Davoudi-Dehaghani Elham, Zeinali Sirous

Abstract excerpt

BACKGROUND: Hemophilia A (HA) is an X-linked recessive bleeding disorder with a high rate of genetic heterogeneity. The present study was conducted on a large cohort of Iranian HA patients and data obtained from databases. METHODS: A total of 622 Iranian HA patients from 329 unrelated families who had been referred to a medical genetics laboratory in Tehran from 2005 to 2019, were enrolled in this retrospective,...

Topics

Factor VIII
Hemophilia A
Humans
Iran
Mutation
Retrospective Studies

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 35014236
DOI: 10.34172/aim.2021.133

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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