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Publikováno v:
Journal of Cellular and Molecular Medicine
Urea cycle disorders (UCDs) are a group of rare metabolic conditions characterized by hyperammonemia and a broad spectrum of phenotypic severity. They are caused by the congenital deficiency in the eight biomolecules involved in urea cycle. In the pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e31ee2226da199b5f06e5230b21bf05
https://pubmed.ncbi.nlm.nih.gov/33611823
https://pubmed.ncbi.nlm.nih.gov/33611823
