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Molecular genetics of β-thalassemia: A narrative review

β-thalassemia is a hereditary hematological disease caused by over 350 mutations in the β-globin gene (HBB). Identifying the genetic variants affecting fetal hemoglobin (HbF) production combined with the α-globin genotype provides some prediction of disease severity for β-thalassemia. However, the g...

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Detalles Bibliográficos
Autores principales:	Jaing, Tang-Her, Chang, Tsung-Yen, Chen, Shih-Hsiang, Lin, Chen-Wei, Wen, Yu-Chuan, Chiu, Chia-Chi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2021
Materias:	4800
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8589257/ https://www.ncbi.nlm.nih.gov/pubmed/34766559 http://dx.doi.org/10.1097/MD.0000000000027522

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