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pro vyhledávání: '"Kátia E.F.A. Coelho"'
Autor:
Kátia E.F.A. Coelho, Mônica M. M. Navarro, Fabrício D. Ventura, Carlos E. Speck-Martins, Daniel R. Carvalho, Jaime M. Brum, Dalton Portugal, Riccardo Pratesi
Publikováno v:
Pediatric Neurology. 46:369-374
Hyperargininemia is an autosomal recessive metabolic disorder caused by a deficiency of enzyme arginase I. It is a rare pan-ethnic disease with a clinical presentation distinct from that of other urea cycle disorders, and hyperammonemic encephalopath
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::868467a35015c2b3ea379a333262ee26
https://doi.org/10.1016/j.pediatrneurol.2012.03.016
https://doi.org/10.1016/j.pediatrneurol.2012.03.016
