Genotype Hemophilia Screening Program Identified 2 Novel Variants Including a Novel Variant (c.5816-2A > G) Causing a Pathogenic Variant of the Factor 8 Gene

Establishing a national screening program for hemophilia patients is highly encouraged by the World Health Organization and the World Federation of Hemophilia. Hence, this study aimed to analyze the variant spectrum of F8 and F9 genes in Arab hemophilia patients. Molecular genetic and sequencing stu...

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Detalles Bibliográficos
Autores principales: Owaidah, Tarek, Bakr, Salwa, Al-Numair, Nouf, AbaAlkhail, Hala, Alzahrani, Hazzaa, Saleh, Mahasen, Khogeer, Haitham, Tarawah, Ahmed, Akkad, Hadeel, Al-Allaf, Faisal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Original Manuscript
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395182/
https://www.ncbi.nlm.nih.gov/pubmed/37525882
http://dx.doi.org/10.1177/10760296231182410

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395182/
https://www.ncbi.nlm.nih.gov/pubmed/37525882
http://dx.doi.org/10.1177/10760296231182410

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