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Dent's disease complicated by nephrotic syndrome: A case report
Dent's disease is an X-linked recessive proximal tubular disorder that mostly affects male patients in childhood or early adult life. The condition is caused by mutations in the CLCN5 (Dent disease 1) or OCRL (Dent disease 2) genes located on chromosome Xp11.22 and Xq25, respectively. In most m...
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| Publicado no: | Intractable Rare Dis Res |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5116868/ https://ncbi.nlm.nih.gov/pubmed/27904828 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2016.01058 |
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