Correction to: Genetics in Medicine 22:2020; https://doi.org/10.1038/s41436-019-0680-1; Article published online 04 November 2019
In the original version of this Article there was a nomenclature error in Table 2 and Supplementary Table S1. For patient 30 it should read c.[2863C>T];[3082+1G>C] and not c.[2863C>T];[3082+1C>G]. This has now been corrected in both the PDF and HTML versions of the Article as well as the supplementary information file.
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Authors and Affiliations
University of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany
Matthias Pergande MSc, Özkan Özdemir PhD, Mona Kreutzer, Haicui Wang PhD, Hülya-Sevcan Daimagüler MSc, Kerstin Becker PhD, Mert Karakaya MD, Janine Altmüller MD, Peter Nürnberg PhD, Prof & Sebahattin Cirak MD
University of Cologne, University Hospital Cologne and Faculty of Medicine, Department of Pediatrics, Cologne, Germany
Matthias Pergande MSc, Özkan Özdemir PhD, Mona Kreutzer, Haicui Wang PhD, Hülya-Sevcan Daimagüler MSc, Kerstin Becker PhD, Anne Koy MD & Sebahattin Cirak MD
University of Cologne, Cologne Center for Genomics CCG, Cologne, Germany
Susanne Motameny PhD, Amit Kawalia PhD, Janine Altmüller MD, Peter Nürnberg PhD, Prof & Holger Thiele MD
University of Cologne, University Hospital Cologne, Institute of Human Genetics, Cologne, Germany
Mert Karakaya MD & Raoul Heller MD, PhD
Department of General Pediatrics and Neonatology, Justus-Liebig-University, Gießen, Germany
Harald Ehrhardt MD & Cho-Ming Chao MD, PhD
Department of Pediatric Genetics, Marmara University Medical School, Istanbul, Turkey
Nursel Elcioglu MD, Prof
Eastern Mediterranean University Medical School, Mersin, Turkey
Nursel Elcioglu MD, Prof
Department of Neurology, Mother and Child Health Care Institute of Serbia “Dr. Vukan Cupic”, Belgrade, Serbia
Slavica Ostojic MD
Department of Pediatric Neurology, Akdeniz University Hospital, Antalya, Turkey
Özgür Duman MD, Prof
Department of Pediatric Neurology, Social Pediatrics and Epileptology, Justus-Liebig-University, Gießen, Germany
Andreas Hahn MD, Prof
Department of Neurology, Rheinische Friedrich-Wilhelms-University, Bonn, Germany
Jens Reimann MD
Institute of Pathology, Philipps University of Marburg, Marburg, Germany
Katharina Schoner MD
Institute of Neuropathology, Justus-Liebig-University, Gießen, Germany
Anne Schänzer MD
Heidelberg University, University Children’s Hospital Heidelberg, Department of Pediatrics, Heidelberg, Germany
Jens H. Westhoff MD
Institute of Human Genetics, Heidelberg University, Institute of Human Genetics, Heidelberg, Germany
Eva Maria Christina Schwaibold MD
University of Montpellier, University Hospital of Montpellier, Molecular Diagnostic Laboratory, Montpellier, France
Mireille Cossee MD
University of Montpellier, University Hospital of Montpellier, Medical Genetics Department, Montpellier, France
Marion Imbert-Bouteille MSc
Johannes-Gutenberg University Mainz, University Medical Center Mainz, Institute of Neuropathology, Mainz, Germany
Harald von Pein MD
Hacettepe University, Children’s Hospital, Department of Pediatric Neurology, Ankara, Turkey
Göknur Haliloglu MD, Prof & Haluk Topaloglu MD, Prof
Genetic Health Service NZ—Northern Hub, Auckland City Hospital, Auckland, New Zealand
Raoul Heller MD, PhD
University of Cologne, Center for Rare Diseases Cologne (ZSEK), Cologne, Germany
Raoul Heller MD, PhD & Sebahattin Cirak MD
- Matthias Pergande MSc
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- Susanne Motameny PhD
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Correspondence to Sebahattin Cirak MD.
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Pergande, M., Motameny, S., Özdemir, Ö. et al. Correction: The genomic and clinical landscape of fetal akinesia. Genet Med 22, 1426–1428 (2020). https://doi.org/10.1038/s41436-020-0839-9
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DOI: https://doi.org/10.1038/s41436-020-0839-9
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