Katarina Peklaj
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Explore the profile of Katarina Peklaj including associated specialties, affiliations and a list of published articles.
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Recent Articles
1.
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...