Author:
Klaassen K.,Djordjevic M.,Skakic A.,Kecman B.,Drmanac R.,Pavlovic S.,Stojiljkovic M.
Funder
Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja
Subject
Endocrinology,Genetics,Molecular Biology
Reference49 articles.
1. Hyperphenylalaninemia: phenylalanine hydroxylase deficiency;Scriver,2008
2. An evaluation of the treatment of phenylketonuria with diets low in phenylalanine;Knox;Pediatrics,1960
3. Metabolic control during the neonatal period in phenylketonuria: associations with childhood IQ;Liemburg;Pediatr Res,2021
4. Can untreated PKU patients escape from intellectual disability? A systematic review;van Vliet;Orphanet J Rare Dis.,2018
5. Molecular genetics and genotype-based estimation of BH4-responsiveness in serbian PKU patients: spotlight on phenotypic implications of pL48S;Djordjevic,2013
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