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- W2023004280 abstract "α thalassemia (α-thal) is one of the most common hemoglobin (Hb) disorders in the world.1 α-globin genes are located on chromosome 16. The majority of α-thal mutations are deletions but point mutations are found as well.2 Since the Iranian population is a mixture of different ethnic groups, frequency and distribution of α-globin mutations in various regions of the country need to be clarified. These findings can contribute to a wider understanding of this disorder." @default.
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- W2023004280 date "2007-07-01" @default.
- W2023004280 modified "2023-09-23" @default.
- W2023004280 title "Elucidating the spectrum of -thalassemia mutations in Iran" @default.
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- W2023004280 doi "https://doi.org/10.3324/haematol.10658" @default.
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