Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1
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Published:2023-11
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ISSN:1079-9796
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Container-title:Blood Cells, Molecules, and Diseases
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