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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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| Pubblicato in: | J Cell Mol Med |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6815805/ https://ncbi.nlm.nih.gov/pubmed/31472005 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.14590 |
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