The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia A

Sarah Azadmehr ¹ , 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 * , Sirous Zeinali ^1,2 *

Cited by CrossRef: 2

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. Pediatric Hematology/Oncology and Immunopathology. 2023;22(3):48 [Crossref]

2- Zuccherato L, Souza R, Camelo R, Santana M, Dias M, Jardim L, de Oliveira A, Lorenzato C, Cerqueira M, Franco V, de Albuquerque Ribeiro R, Etto L, Roberti M, de Araújo Callado F, de Cerqueira M, de Souza Pinto I, Garcia A, Anegawa T, Neves D, Chaves D, Rezende S. Deleterious variants cluster in the A3 domain of factor VIII in people with severe hemophilia A and inhibitors. Research and Practice in Thrombosis and Haemostasis. 2025;9(6):103006 [Crossref]

3- 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.