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Arch Iran Med. 2021;24(12): 887-896. doi: 10.34172/aim.2021.133

Original Article

The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia A

Sarah Azadmehr 1 ORCID, Faezeh Rahiminejad 1, Fatemeh Zafarghandi Motlagh 1, Mojdeh Jamali 1, Pardis Ghazizadeh Tehrani 1, Tina Shirzadeh 1, Hamideh Bagherian 1, Morteza Karimipoor 2, Elham Davoudi-Dehaghani 2 * ORCID, Sirous Zeinali 1,2 * ORCID

Cited by CrossRef: 1

1- Liubushkin A, Guryanova I, Dmitriev E, Vertelko V, Polyakova E, Volkova L, Aleinikova O. Molecular genetic diagnosis in the group of hemophilia A patients in Belarus: 12 new allelic variants in the F8 gene. Voprosy gematologii/onkologii i immunopatologii v pediatrii. 2023;22(3):48 [Crossref]
2- Pshenichnikova O, Salomashkina V, Poznyakova J, Selivanova D, Chernetskaya D, Yakovleva E, Dimitrieva O, Likhacheva E, Perina F, Zozulya N, Surin V. Spectrum of Causative Mutations in Patients with Hemophilia A in Russia. Genes. 2023;14(2):260 [Crossref]

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A Monthly Peer-Reviewed Medical Journal Published by the Academy of Medical Sciences of the I.R. Iran; Indexed in PubMed/MEDLINE, ISI Web of Science, EMBASE, SCOPUS, CINHAL, PASCAL, CSA, SID, ISSN: Print 1029-2977, Online 1735-3947.The impact factor of Archives of Iranian Medicine according to Journal Citation Reports® (JCR®) 2016 is 1.20.