Genetic Variations of ferroportin-1(FPN1-8CG), TMPRSS6 (rs855791) and Hemojuvelin (I222N and G320V) Among a Cohort of Egyptian β-Thalassemia Major Patients

Iron overload remains a major cause of morbidity and mortality among β-thalassemia major (β-TM) patients. Iron regulatory proteins and their genetic variants together with changes in hepcidin levels in thalassemic patients could affect the disease manifestations. This work aimed to study genetic var...

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Detalles Bibliográficos
Autores principales: El-Gharbawi, Nesrine, Shaheen, Iman, Hamdy, Mona, Elgawhary, Somaya, Samir, Mohamed, Hanna, Baher Matta, Ali, Eman Yousief, Youssef, Eman Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10064347/
https://www.ncbi.nlm.nih.gov/pubmed/37006987
http://dx.doi.org/10.1007/s12288-022-01580-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10064347/
https://www.ncbi.nlm.nih.gov/pubmed/37006987
http://dx.doi.org/10.1007/s12288-022-01580-8

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