Author:
Beghini Marianna,Pichler Maximilian,Tinnefeld Fiona Carolina,Metz Matthäus,Möslinger Dorothea,Konstantopoulou Vassiliki,Spenger Johannes,Kautzky-Willer Alexandra,Frommlet Florian,Scherer Thomas,Hufgard-Leitner Miriam
Reference14 articles.
1. The genetic landscape and epidemiology of phenylketonuria;Hillert;Am. J. Hum. Genet.,2020
2. Phenylketonuria: an inborn error of phenylalanine metabolism;Williams;Clin. Biochem. Rev.,2008
3. Psychiatric and cognitive aspects of phenylketonuria: the limitations of diet and promise of new treatments;Ashe;Front. Psychol.,2019
4. Characterisation and differential diagnosis of neurological complications in adults with phenylketonuria: literature review and expert opinion;Merkel;J. Neurol.,2023
5. Phenylalanine hydroxylase deficiency: diagnosis and management guideline;Vockley;Genet. Med.,2014