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Autor:
Sali Usher, Tova Morad, Elena Keren-Tardai, Hava Peretz, Hanna Shalev, Ayala Lagziel, Daniel Landau, Tong Zhang, Gavin Blackburn, David Levartovsky, David G. Watson, Victoria Greenshpun, Meirav Shtauber-Naamati
Publikováno v:
Metabolomics. 8:951-959
Classical xanthinuria is a rare inherited metabolic disorder caused by either isolated xanthine dehydrogenase (XDH) deficiency (type I) or combined XDH and aldehyde oxidase (AO) deficiency (type II). XDH and AO are evolutionary related enzymes that s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbcb4c797c253f2afe37efc305d151de
https://doi.org/10.1007/s11306-011-0391-3
https://doi.org/10.1007/s11306-011-0391-3
