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Publikováno v:
International Journal of Medical Reviews and Case Reports. :1
Introduction The deficiency in ornithine carbamyl transferase (OCT) is an enzyme deficiency transmitted in the recessive or dominant mode associated with X. Complete deficit is still expressed in hemizygous boys in a very severe and often fatal neona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6893372abb46a3e7e5462343f0985cb8
https://doi.org/10.5455/ijmrcr.metabolic-disease-ornithine-carbamyl-tranferase
https://doi.org/10.5455/ijmrcr.metabolic-disease-ornithine-carbamyl-tranferase
