Browsing by Subject "4-hydroxyphenylpyruvate dioxygenase, alkaptonuria, homogentisate dioxygenase, nitisinone, ReCore"
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Identification of Potential Inhibitors for the Treatment of Alkaptonuria Using an Integrated In Silico Computational Strategy
(NLM (Medline), 2023)Alkaptonuria (AKU) is a rare genetic autosomal recessive disorder characterized by elevated serum levels of homogentisic acid (HGA). In this disease, tyrosine metabolism is interrupted because of the alterations in ...