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- W2788407440 abstract "Thalassemia is a disorder of hemoglobin characterized by reduced or absent production of one of the globin chains in human red blood cells with relative excess of the other. Impaired synthesis of β-globin results in β-thalassemia, whereas defective synthesis of α-globin leads to α-thalassemia. Despite being a monogenic disorder , thalassemia exhibits remarkable clinical heterogeneity that is directly related to the intracellular imbalance between α- and β-like globin chains. Novel insights into the genetic modifiers have contributed to the understanding of the correlation between genotype and phenotype and are being explored as therapeutic pathways to cure this life-limiting disease." @default.
- W2788407440 created "2018-03-06" @default.
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- W2788407440 date "2018-04-01" @default.
- W2788407440 modified "2023-10-11" @default.
- W2788407440 title "Molecular Basis and Genetic Modifiers of Thalassemia" @default.
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- W2788407440 doi "https://doi.org/10.1016/j.hoc.2017.11.003" @default.
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