Comprehensive characterization of ureagenesis in the spf

Autor:	Gabriella, Allegri, Sereina, Deplazes, Nicole, Rimann, Benjamin, Causton, Tanja, Scherer, Jonathan W, Leff, Carmen, Diez-Fernandez, Anna, Klimovskaia, Ralph, Fingerhut, Jakub, Krijt, Viktor, Kožich, Jean-Marc, Nuoffer, Hiu M, Grisch-Chan, Beat, Thöny, Johannes, Häberle
Rok vydání:	2018
Předmět:	Male Aging Age Factors Mice Transgenic Ornithine Carbamoyltransferase Deficiency Disease Disease Models Animal Mice Liver Ammonia Animals Humans Hyperammonemia Urea Ornithine Carbamoyltransferase
Zdroj:	Journal of inherited metabolic diseaseREFERENCES. 42(6)
ISSN:	1573-2665
Popis:	The most common ureagenesis defect is X-linked ornithine transcarbamylase (OTC) deficiency which is a main target for novel therapeutic interventions. The spf
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::a19c76c7151222ee78218d1e07ea8d94 https://pubmed.ncbi.nlm.nih.gov/30714172 Zobrazit plný text záznamu Full text from SpringerLink Plný text