Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency

Wortmann, Saskia B.; Ziętkiewicz, Szymon; Guerrero-Castillo, Sergio; Feichtinger, René G.; Wagner, Matias; Russell, Jacqui; Ellaway, Carolyn; Mróz, Dagmara; Wyszkowski, Hubert; Weis, Denisa; Hannibal, Iris; von Stülpnagel, Celina; Cabrera-Orefice, Alfredo; Lichter-Konecki, Uta; Gaesser, Jenna; Windreich, Randy; Myers, Kasiani C.; Lorsbach, Robert; Dale, Russell C.; Gersting, Søren; Prada, Carlos E.; Christodoulou, John; Wolf, Nicole I.; Venselaar, Hanka; Mayr, Johannes A.; Wevers, Ron A.

doi:10.1038/s41436-021-01280-0

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Correction
Published: 23 July 2021

Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency

Saskia B. Wortmann ORCID: orcid.org/0000-0002-1968-8103^1,2,3^na1,
Szymon Ziętkiewicz⁴^na1,
Sergio Guerrero-Castillo⁵^na2,
René G. Feichtinger¹^na2,
Matias Wagner^6,7,
Jacqui Russell⁸,
Carolyn Ellaway^8,9,10,
Dagmara Mróz⁴,
Hubert Wyszkowski⁴,
Denisa Weis¹¹,
Iris Hannibal¹²,
Celina von Stülpnagel^12,13,
Alfredo Cabrera-Orefice¹⁴,
Uta Lichter-Konecki^15,16,
Jenna Gaesser^15,16,
Randy Windreich^16,17,
Kasiani C. Myers^18,19,
Robert Lorsbach^18,20,
Russell C. Dale²¹,
Søren Gersting⁵,
Carlos E. Prada^18,22,
John Christodoulou^9,10,23,
Nicole I. Wolf^24,25,
Hanka Venselaar¹⁴,
Johannes A. Mayr¹ &
…
Ron A. Wevers^3,26

Genetics in Medicine volume 23, page 1789 (2021)Cite this article

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The Original Article was published on 17 June 2021

Correction to: Genetics in Medicine 2021; https://doi.org/10.1038/s41436-021-01194-x; published online 17 June 2021

Unfortunately the funding information was not given. Funding is as follows: This work was funded by the ERA PerMed project PerMiM (Austrian Science Fund FWF, I4704-B) to S.B.W.

This study was supported by a “Sonata Bis 5” grant of the National Science Center Poland (2015/18/E/NZ1/00673) to S.Z. and D.M.

Author information

These authors contributed equally: Saskia B. Wortmann, Szymon Ziętkiewicz.
These authors contributed equally: Sergio Guerrero-Castillo, René G. Feichtinger.

Authors and Affiliations

University Children’s Hospital, Paracelsus Medical University (PMU), Salzburg, Austria
Saskia B. Wortmann, René G. Feichtinger & Johannes A. Mayr
Radboud Center for Mitochondrial Medicine, Department of Pediatrics, Amalia Children’s Hospital, Radboudumc, Nijmegen, The Netherlands
Saskia B. Wortmann
United for Metabolic Diseases (UMD), Amsterdam, The Netherlands
Saskia B. Wortmann & Ron A. Wevers
Intercollegiate Faculty of Biotechnology, University of Gdansk, Gdansk, Poland
Szymon Ziętkiewicz, Dagmara Mróz & Hubert Wyszkowski
University Children’s Research@Kinder-UKE, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Sergio Guerrero-Castillo & Søren Gersting
Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg, Germany
Matias Wagner
Institute of Human Genetics, Technical University of Munich, Munich, Germany
Matias Wagner
Genetic Metabolic Disorders Service, Sydney Children’s Hospital Network, Randwick, NSW, Australia
Jacqui Russell & Carolyn Ellaway
Discipline of Child & Adolescent Health; Sydney Medical School, University of Sydney, Sydney, NSW, Australia
Carolyn Ellaway & John Christodoulou
Discipline of Genetic Medicine, Sydney Medical School, University of Sydney, Sydney, NSW, Australia
Carolyn Ellaway & John Christodoulou
Department of Medical Genetics, Med Campus IV, Kepler University Hospital, Johannes Kepler University, Linz, Austria
Denisa Weis
Division of Pediatric Neurology, Developmental Medicine and Social Pediatrics, Department of Pediatrics, Dr. von Hauner Children’s Hospital, Ludwig-Maximilians-University, Munich, Germany
Iris Hannibal & Celina von Stülpnagel
Institute for Transition, Rehabilitation and Palliation, Paracelsus Medical University, Salzburg, Austria
Celina von Stülpnagel
Center for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences (RIMLS), Nijmegen, The Netherlands
Alfredo Cabrera-Orefice & Hanka Venselaar
Children’s Hospital of Pittsburgh, Pittsburgh, PA, USA
Uta Lichter-Konecki & Jenna Gaesser
Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA
Uta Lichter-Konecki, Jenna Gaesser & Randy Windreich
Division of Blood and Marrow Transplantation and Cellular Therapies, UPMC Children’s Hospital of Pittsburgh, Pittsburgh, PA, USA
Randy Windreich
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA
Kasiani C. Myers, Robert Lorsbach & Carlos E. Prada
Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
Kasiani C. Myers
Division of Pathology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
Robert Lorsbach
Neuroimmunology Group, Institute for Neuroscience and Muscle Research, Kids Research Institute at the Children’s Hospital at Westmead, University of Sydney, Sydney, Australia
Russell C. Dale
Division of Human Genetics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
Carlos E. Prada
Murdoch Children’s Research Institute and Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia
John Christodoulou
Department of Child Neurology, Amsterdam Leukodystrophy Center, Emma Children’s Hospital, Amsterdam UMC, Amsterdam, The Netherlands
Nicole I. Wolf
Amsterdam Neuroscience, Vrije Universiteit, Amsterdam, The Netherlands
Nicole I. Wolf
Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands
Ron A. Wevers

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Saskia B. Wortmann
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Szymon Ziętkiewicz
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Sergio Guerrero-Castillo
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René G. Feichtinger
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Matias Wagner
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Jacqui Russell
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Carolyn Ellaway
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Dagmara Mróz
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Hubert Wyszkowski
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Denisa Weis
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Iris Hannibal
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Celina von Stülpnagel
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Alfredo Cabrera-Orefice
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Jenna Gaesser
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Randy Windreich
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Kasiani C. Myers
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Robert Lorsbach
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Russell C. Dale
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Søren Gersting
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Hanka Venselaar
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Johannes A. Mayr
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Ron A. Wevers
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Correspondence to Saskia B. Wortmann.

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Wortmann, S.B., Ziętkiewicz, S., Guerrero-Castillo, S. et al. Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency. Genet Med 23, 1789 (2021). https://doi.org/10.1038/s41436-021-01280-0

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Published: 23 July 2021
Issue date: September 2021
DOI: https://doi.org/10.1038/s41436-021-01280-0

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