Inducible Arginase 1 Deficiency in Mice Leads to Hyperargininemia and Altered Amino Acid Metabolism

Arginase deficiency is a rare autosomal recessive disorder resulting from a loss of the liver arginase isoform, arginase 1 (ARG1), which is the final step in the urea cycle for detoxifying ammonia. ARG1 deficiency leads to hyperargininemia, characterized by progressive neurological impairment, persi...

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Xehetasun bibliografikoak
Egile Nagusiak: Sin, Yuan Yan, Ballantyne, Laurel L., Mukherjee, Kamalika, St. Amand, Tim, Kyriakopoulou, Lianna, Schulze, Andreas, Funk, Colin D.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Public Library of Science 2013
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3817112/
https://ncbi.nlm.nih.gov/pubmed/24224027
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0080001
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