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Nephronophthisis
Nephronophthisis (NPHP) is an autosomal recessive cystic kidney disease, which represents the most frequent genetic cause for end-stage renal disease up to the third decade of life. Nephronophthisis is caused by mutations in eleven different genes called nephrocystins (NPHP1-11, NPHP1L). With an inc...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4160028/ https://ncbi.nlm.nih.gov/pubmed/20652329 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-010-1585-z |
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