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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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Detalhes bibliográficos
Main Authors: Knight, John, Holmes, Ross P., Cramer, Scott D., Takayama, Tatsuya, Salido, Eduardo
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2012
Assuntos:
Acesso em linha: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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