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Hydroxyproline metabolism in mouse models of primary hyperoxaluria
Primary hyperoxaluria type 1 (PH1) and type 2 (PH2) are rare genetic diseases that result from deficiencies in glyoxylate metabolism. The increased oxalate synthesis that occurs can lead to kidney stone formation, deposition of calcium oxalate in the kidney and other tissues, and renal failure. Hydr...
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| Auteurs principaux: | , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
American Physiological Society
2012
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3311317/ https://ncbi.nlm.nih.gov/pubmed/22189945 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajprenal.00473.2011 |
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