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- W2912653529 abstract "Beta-thalassemia (β-thal) is an inherited hemoglobin disorder, characterized by the absence of or reduced hemoglobin chains that result in microcytic hypochromic anemia. In this case, we describe a..." @default.
- W2912653529 created "2019-02-21" @default.
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- W2912653529 date "2019-01-01" @default.
- W2912653529 modified "2023-09-25" @default.
- W2912653529 title "A compound heterozygous −29 A>G and IVS-I-1 G>A mutation of HBB gene leading to β-thalassemia intermedia in a Syrian patient: A case report" @default.
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- W2912653529 doi "https://doi.org/10.1080/2331205x.2019.1581448" @default.
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