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 <em>PIEZO1</em>, <em>Spectrin ß1</em>, <em>RhAG</em> and <em>SLC4A1</em>

Publication date: Available online 20 July 2023Source: Blood Cells, Molecules, and DiseasesAuthor(s): Benoit Allegrini, Ludivine David NGuyen, Morgane Mignotet, Catherine Etchebest, Odile Fenneteau, Jessica Platon, Anne Lambilliotte, Hélène Guizouarn, …