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Katarina Peklaj

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Gregoric N, Tara A, Kastelic R, Sikonja J, Peklaj K, Mesojedec M, et al.
Mol Genet Metab Rep . 2024 Jul; 40:101115. PMID: 39049877
Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine (Phe) metabolism, resulting from the deficient activity of phenylalanine hydroxylase that converts Phe to tyrosine in the liver, leading to...