Cargando…
New KCNN4 Variants Associated With Anemia: Stomatocytosis Without Erythrocyte Dehydration
The K(+) channel activated by the Ca(2+), KCNN4, has been shown to contribute to red blood cell dehydration in the rare hereditary hemolytic anemia, the dehydrated hereditary stomatocytosis. We report two de novo mutations on KCNN4, We reported two de novo mutations on KCNN4, V222L and H340N, charac...
Autores principales: | Allegrini, B., Jedele, S., David Nguyen, L., Mignotet, M., Rapetti-Mauss, R., Etchebest, C., Fenneteau, O., Loubat, A., Boutet, A., Thomas, C., Durin, J., Petit, A., Badens, C., Garçon, L., Da Costa, L., Guizouarn, H. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393219/ https://www.ncbi.nlm.nih.gov/pubmed/36003639 http://dx.doi.org/10.3389/fphys.2022.918620 |
Ejemplares similares
-
Variant spectrum of PIEZO1 and KCNN4 in Japanese patients with dehydrated hereditary stomatocytosis
por: Nakahara, Erina, et al.
Publicado: (2023) -
Dehydrated hereditary stomatocytosis: clinical perspectives
por: Frederiksen, Henrik
Publicado: (2019) -
Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family
por: Waldstein, Sasha, et al.
Publicado: (2021) -
Hereditary Xerocytosis: Differential Behavior of PIEZO1 Mutations in the N-Terminal Extracellular Domain Between Red Blood Cells and HEK Cells
por: Yamaguchi, Yohei, et al.
Publicado: (2021) -
Band 3 Missense Mutations and Stomatocytosis: Insight into the Molecular Mechanism Responsible for Monovalent Cation Leak
por: Barneaud-Rocca, Damien, et al.
Publicado: (2011)