KCC3a, a Strong Candidate Pathway for K(+) Loss in Alkalemia

Loss-of-function mutations in the human potassium chloride cotransporter-3 (KCC3) cause a hereditary motor sensory neuropathy associated with agenesis of the corpus callosum. While recapitulating the neuropathy, KCC3-knockout mice also exhibit high blood pressure. This phenotype is believed to have...

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Detalles Bibliográficos
Autores principales: Ferdaus, Mohammed Zubaerul, Terker, Andrew Scott, Koumangoye, Rainelli, Delpire, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301082/
https://www.ncbi.nlm.nih.gov/pubmed/35874803
http://dx.doi.org/10.3389/fcell.2022.931326

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301082/
https://www.ncbi.nlm.nih.gov/pubmed/35874803
http://dx.doi.org/10.3389/fcell.2022.931326

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