Rare and New Mutations of B-Globin in Azari Population of Iran, a Considerable Diversity

BACKGROUND: Thalassemia, as the most common single-gene genetic disorder, is related to a defect in the synthesis of one or more hemoglobin chains. More than 200 mutations have been identified in the β-globin gene. Globally, every susceptible racial group has its own specific spectrum of the common...

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Detalles Bibliográficos
Autores principales: Abbasali, F.H., Mahmoud, K.Sh., Hengameh, N., Mina, D.H., Setare, D., Hale, D.M, Sima, D.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230832/
https://www.ncbi.nlm.nih.gov/pubmed/37265972
http://dx.doi.org/10.2478/bjmg-2022-0016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230832/
https://www.ncbi.nlm.nih.gov/pubmed/37265972
http://dx.doi.org/10.2478/bjmg-2022-0016

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