Dihydropyrimidinase Deficiency: The First Feline Case of Dihydropyrimidinuria with Clinical and Molecular Findings

Dihydropyrimidinase (DHP, EC 3.5.2.2) is the second enzyme of the pyrimidine degradation pathway and a deficiency of this enzyme is responsible for a rare inborn metabolic syndrome characterized by dihydropyrimidinuria. Here we report a cat with DHP deficiency, manifesting malnutrition, depression,...

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Detaylı Bibliyografya
Asıl Yazarlar: Chang, Hye-Sook, Shibata, Takako, Arai, Satoshi, Zhang, Chunhua, Yabuki, Akira, Mitani, Sawane, Higo, Takashi, Sunagawa, Kazuhiro, Mizukami, Keijiro, Yamato, Osamu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Springer Berlin Heidelberg 2012
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3565656/
https://ncbi.nlm.nih.gov/pubmed/23430934
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2012_139
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