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Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia.
Hematology. 2023 Dec;28(1):2187155. doi: 10.1080/16078454.2023.2187155.
Hematology. 2023.
PMID: 36939018
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