Association of Genetic Variant FVIII Gene and Factor VIII: A Pilot Study Among Hemophilia A Female Relatives in Saudi Arabia

Hemophilia A (HA) is an X-linked recessive disorder that results from mutations in the factor VIII gene (FVIII). Most affected patients are males due to the inheritance of mutations in the FVIII gene from their mothers. Females are mostly found to be carriers unless they inherited the mutation from...

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Detalles Bibliográficos
Autores principales: Almohammadi, Abdullah T, Radhwi, Osman, AlAhwal, Hatem, Barefah, Ahmed, Bahashwan, Salem, Ashankyty, Ibraheem M, Almashjari, Majed, Ayaz, Rawan, Al-Marzouki, Adel, Zaher, Galila F, Hussain, Hend, Samman, Abeer A, Zakariyah, Abeer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10431930/
https://www.ncbi.nlm.nih.gov/pubmed/37593302
http://dx.doi.org/10.7759/cureus.42038

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10431930/
https://www.ncbi.nlm.nih.gov/pubmed/37593302
http://dx.doi.org/10.7759/cureus.42038

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