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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)....
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Materias: | |
| 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 |