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Publikováno v:
Romanian Journal of Diabetes Nutrition and Metabolic Diseases. 19:215-218
Galactosemia is a hereditary metabolic disease, having autosomal recessivetransmission. It can be the result of three distinct enzyme deficits on the path ofgalactose metabolism: Galactose-1-phosphate uridylyltransferase (GALT),Galactokinase and UDP-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0cbd14035a611ea81261f336ae01b55
https://doi.org/10.2478/v10255-012-0026-0
https://doi.org/10.2478/v10255-012-0026-0
