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Inactivation of Bardet-Biedl syndrome genes causes kidney defects
Bardet-Biedl syndrome (BBS) is a rare hereditary autosomal recessive disease associated with several features including obesity, hypertension, and renal abnormalities. The underlying mechanisms of renal defects associated with BBS remain poorly defined. We examined the histological, molecular, and f...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Physiological Society
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3043995/ https://ncbi.nlm.nih.gov/pubmed/21106857 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajprenal.00150.2010 |
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