Correction to: DNAJC12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant.

Autor: Çıkı K; Division of Pediatric Metabolism, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey. kismet.ciki@hacettepe.edu.tr., Yıldız Y; Division of Pediatric Metabolism, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey., Yücel Yılmaz D; Department of Pediatric Metabolism, Institute of Child Health, Hacettepe University, Ankara, Turkey., Pektaş E; Pediatric Metabolic Diseases Unit, Gaziantep Cengiz Gökçek Maternity and Pediatrics Hospital, Gaziantep, Turkey., Tokatlı A; Division of Pediatric Metabolism, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey., Özgül RK; Department of Pediatric Metabolism, Institute of Child Health, Hacettepe University, Ankara, Turkey., Sivri HS; Division of Pediatric Metabolism, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey., Dursun A; Division of Pediatric Metabolism, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Jazyk: angličtina
Zdroj: Metabolic brain disease [Metab Brain Dis] 2021 Aug; Vol. 36 (6), pp. 1411.
DOI: 10.1007/s11011-021-00759-8
Abstrakt: A Correction to this paper has been published: https://doi.org/10.1007/s11011-021-00759-8.
(© 2021. Springer Science+Business Media, LLC, part of Springer Nature.)
Databáze: MEDLINE
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