Correction to: The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype

Affiliations

• ¹ Institute of Human Genetics, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Universitätsstraße 1, 40225, Düsseldorf, Germany.
• ² Department of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.
• ³ Division of Bioinformatics, Institute of Biochemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
• ⁴ Children's Hospital Datteln, University Witten Herdecke, Datteln, Germany.
• ⁵ Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
• ⁶ Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
• ⁷ Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
• ⁸ Division of Medical Genetics, Department of Pediatrics, DuPont Hospital for Children, Nemours Alfred I, Wilmington, Delaware, DE, USA.
• ⁹ Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, The National Hospital for Neurology and Neurosurgery, London, UK.
• ¹⁰ Institute of Human Genetics, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Universitätsstraße 1, 40225, Düsseldorf, Germany. dagmar.wieczorek@hhu.de.