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Hydroxyproline metabolism in a mouse model of Primary Hyperoxaluria Type 3
Primary Hyperoxaluria Type 3 is a recently discovered form of this autosomal recessive disease that results from mutations in the gene coding for 4-hydroxy-2-oxoglutarate aldolase (HOGA1). This enzyme is one of the 2 unique enzymes in the hydroxyproline catabolism pathway. Affected individuals have...
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| Publicado no: | Biochim Biophys Acta |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4615548/ https://ncbi.nlm.nih.gov/pubmed/26428388 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbadis.2015.09.016 |
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