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
| Autor: | Allegrini, Benoit, NGuyen, Ludivine David, Mignotet, Morgane, Etchebest, Catherine, Fenneteau, Odile, Platon, Jessica, Lambilliotte, Anne, Guizouarn, Hélène, Da Costa, Lydie |
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| Zdroj: | In Blood Cells, Molecules and Diseases November 2023 103 |
| Databáze: | ScienceDirect |
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