The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells
Author:
Funder
National Institute for Health Research
NHS Blood and Transplant
Publisher
Frontiers Media SA
Subject
Physiology (medical),Physiology
Reference121 articles.
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1. 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;Blood Cells, Molecules, and Diseases;2023-11
2. The cation‐leaky hereditary stomatocytosis syndromes: A tale of six proteins;British Journal of Haematology;2023-09-07
3. Impact of Familial Pseudohyperkalemia on Donated Blood and Clinical Outcomes from Transfusion;The Korean Journal of Blood Transfusion;2023-08-31
4. Unidirectional fluxes of monovalent ions in human erythrocytes compared with lymphoid U937 cells: Transient processes after stopping the sodium pump and in response to osmotic challenge;PLOS ONE;2023-05-04
5. Marked hyperkalemia due to inappropriate blood sample storage in two suspected cases of familial pseudohyperkalemia;CEN Case Reports;2023-03-12
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