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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Sciendo
2023
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| 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 |