ROMK expression remains unaltered in a mouse model of familial hyperkalemic hypertension caused by the CUL3(Δ403‐459) mutation

Familial hyperkalemic hypertension (FHHt) is a rare inherited form of salt‐dependent hypertension caused by mutations in proteins that regulate the renal Na(+)‐Cl(‐) cotransporter NCC. Mutations in four genes have been reported to cause FHHt including CUL3 (Cullin3) that encodes a component of a RIN...

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Detalles Bibliográficos
Autores principales: Murthy, Meena, Kurz, Thimo, O'Shaughnessy, Kevin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945836/
https://www.ncbi.nlm.nih.gov/pubmed/27378813
http://dx.doi.org/10.14814/phy2.12850

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945836/
https://www.ncbi.nlm.nih.gov/pubmed/27378813
http://dx.doi.org/10.14814/phy2.12850

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