Clinical, genetic, and experimental research of hyperphenylalaninemia
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DOI: 10.3389/fgene.2022.1051153
Abstract: Hyperphenylalaninemia (HPA) is the most common amino acid metabolism defect in humans. It is an autosomal-recessive disorder of the phenylalanine (Phe) metabolism, in which high Phe concentrations and low tyrosine (Tyr) concentrations in the blood… read more here.
Keywords: genetic experimental; experimental research; clinical genetic; hyperphenylalaninemia ... See more keywords