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Alkaptonuria (AKU) is a rare autosomal recessive disorder with an incidence of 1:250 000 to 1:1000 000 live births. AKU is caused by a deficiency of the enzyme homogentisate 1,2-dioxygenase (HGO). This enzyme converts homogentisic acid (HGA) to maley
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9477::805fe92992234e66011c14f22bc030bb
https://hdl.handle.net/20.500.12511/9188
https://hdl.handle.net/20.500.12511/9188
