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Dent disease: A window into calcium and phosphate transport

This review examines calcium and phosphate transport in the kidney through the lens of the rare X‐linked genetic disorder Dent disease. Dent disease type 1 (DD1) is caused by mutations in the CLCN5 gene encoding ClC‐5, a Cl(−)/H(+) antiporter localized to early endosomes of the proximal tubule (PT)....

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Detalles Bibliográficos
Autores principales:	Anglani, Franca, Gianesello, Lisa, Beara‐Lasic, Lada, Lieske, John
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2019
Materias:	Reviews
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815805/ https://www.ncbi.nlm.nih.gov/pubmed/31472005 http://dx.doi.org/10.1111/jcmm.14590

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