Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x)
Por:
Wortmann S.B., Zietkiewicz S., Guerrero-Castillo S., Feichtinger R.G., Wagner M., Russell J., Ellaway C., Mróz D., Wyszkowski H., Weis D., Hannibal I., von Stülpnagel C., Cabrera-Orefice A., Lichter-Konecki U., Gaesser J., Windreich R., Myers K.C., Lorsbach R., Dale R.C., Gersting S., Prada C.E., Christodoulou J., Wolf N.I., Venselaar H., Mayr J.A., Wevers R.A.
Publicada:
1 ene 2021
Resumen:
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. © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics.
Filiaciones:
University Children’s Hospital, Paracelsus Medical University (PMU), Salzburg, Austria
Radboud Center for Mitochondrial Medicine, Department of Pediatrics, Amalia Children’s Hospital, Radboudumc, Nijmegen, Netherlands
United for Metabolic Diseases (UMD), Amsterdam, Netherlands
Intercollegiate Faculty of Biotechnology, University of Gdansk, Gdansk, Poland
University Children’s
Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg, Germany
Institute of Human Genetics, Technical University of Munich, Munich, Germany
Genetic Metabolic Disorders Service, Sydney Children’s Hospital Network, Randwick, NSW, Australia
Discipline of Child & Adolescent Health
Department of Medical Genetics, Med Campus IV, Kepler University Hospital, Johannes Kepler University, Linz, Austria
Division of Pediatric Neurology, Developmental Medicine and Social Pediatrics, Department of Pediatrics, Dr. von Hauner Children’s Hospital, Ludwig-Maximilians-University, Munich, Germany
Institute for Transition, Rehabilitation and Palliation, Paracelsus Medical University, Salzburg, Austria
Center for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences (RIMLS), Nijmegen, Netherlands
Children’s Hospital of Pittsburgh, Pittsburgh, PA, United States
Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States
Division of Blood and Marrow Transplantation and Cellular Therapies, UPMC Children’s Hospital of Pittsburgh, Pittsburgh, PA, United States
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States
Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, United States
Division of Pathology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, United States
Neuroimmunology Group, Institute for Neuroscience and Muscle Research, Kids Research Institute at the Children’s Hospital at Westmead, University of Sydney, Sydney, Australia
Division of Human Genetics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, United States
Department of Child Neurology, Amsterdam Leukodystrophy Center, Emma Children’s Hospital, Amsterdam UMC, Amsterdam, Netherlands
Amsterdam Neuroscience, Vrije Universiteit, Amsterdam, Netherlands
Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, Netherlands
All Open Access; Bronze
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