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-Reference-Cited by-同舟云学术

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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

Published:2023-11 Issue: Volume:103 Page:102780
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Allegrini Benoit,NGuyen Ludivine David,Mignotet Morgane,Etchebest Catherine,Fenneteau Odile,Platon Jessica,Lambilliotte Anne,Guizouarn Hélène,Da Costa Lydie

Funder

Agence Nationale de la Recherche

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference33 articles.

1. Red cell membrane disorders;Narla;Int. J. Lab. Hematol.,2017

2. Advances in understanding the pathogenesis of the red cell volume disorders;Badens;Br. J. Haematol.,2016

3. The molecular basis for altered cation permeability in hereditary stomatocytic human red blood cells;Flatt;Front. Physiol.,2018

4. New insights on hereditary erythrocyte membrane defects;Andolfo;Haematologica,2016

5. Disorders of erythrocyte hydration;Gallagher;Blood,2017

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