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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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Pubblicato in:Biochim Biophys Acta
Autori principali: Li, Xingsheng, Knight, John, Lowther, W. Todd, Holmes, Ross P.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2015
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Accesso online: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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