Correction: Aminoacyl-tRNA synthetase deficiencies in search of common themes

Affiliations

¹ Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands. S.Fuchs@umcutrecht.nl.
² Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
³ Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
⁴ Department of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.
⁵ Department of Pediatric Pulmonology, Academic Medical Center Amsterdam, Amsterdam, The Netherlands.
⁶ Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
⁷ Department of Neonatology, University Medical Center Utrecht, Utrecht, The Netherlands.
⁸ Department of Pediatrics, Maxima Medical Centre Veldhoven, Veldhoven, The Netherlands.
⁹ Department of Child Neurology, VU University Medical Center, Amsterdam, The Netherlands.
¹⁰ Nijmegen Centre for Mitochondrial Disorders at Department of Pediatrics, Radboud University Nijmegen Centre, Nijmegen, The Netherlands.
¹¹ Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
¹² Division of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
¹³ Department of Pediatrics, VU University Medical Center, Amsterdam, The Netherlands.

^# Contributed equally.

Published Erratum

Sabine A Fuchs et al. Genet Med. 2021 Oct.

. 2021 Oct;23(10):2024.

doi: 10.1038/s41436-020-00966-1.

¹ Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands. S.Fuchs@umcutrecht.nl.
² Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
³ Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
⁴ Department of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.
⁵ Department of Pediatric Pulmonology, Academic Medical Center Amsterdam, Amsterdam, The Netherlands.
⁶ Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
⁷ Department of Neonatology, University Medical Center Utrecht, Utrecht, The Netherlands.
⁸ Department of Pediatrics, Maxima Medical Centre Veldhoven, Veldhoven, The Netherlands.
⁹ Department of Child Neurology, VU University Medical Center, Amsterdam, The Netherlands.
¹⁰ Nijmegen Centre for Mitochondrial Disorders at Department of Pediatrics, Radboud University Nijmegen Centre, Nijmegen, The Netherlands.
¹¹ Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
¹² Division of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
¹³ Department of Pediatrics, VU University Medical Center, Amsterdam, The Netherlands.

^# Contributed equally.

No abstract available

Erratum for

Aminoacyl-tRNA synthetase deficiencies in search of common themes.
Fuchs SA, Schene IF, Kok G, Jansen JM, Nikkels PGJ, van Gassen KLI, Terheggen-Lagro SWJ, van der Crabben SN, Hoeks SE, Niers LEM, Wolf NI, de Vries MC, Koolen DA, Houwen RHJ, Mulder MF, van Hasselt PM. Fuchs SA, et al. Genet Med. 2019 Feb;21(2):319-330. doi: 10.1038/s41436-018-0048-y. Epub 2018 Jun 6. Genet Med. 2019. PMID: 29875423 Free PMC article.