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Blok LS, Rousseau J, Twist J, et al. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nat Commun. 2019;10(1):883doi: 10.1038/s41467-019-08800-2.
Blok, L. S., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H., Rodan, L. H., Nowak, C. B., Douglas, J., Swoboda, K. J., Steeves, M. A., Sahai, I., Stumpel, C. T. R. M., Stegmann, A. P. A., Wheeler, P., Willing, M., Fiala, E., Kochhar, A., Gibson, W. T., Cohen, A. S. A., Agbahovbe, R., Innes, A. M., Au, P. Y. B., Rankin, J., Anderson, I. J., Skinner, S. A., Louie, R. J., Warren, H. E., Afenjar, A., Keren, B., Nava, C., Buratti, J., Isapof, A., Rodriguez, D., Lewandowski, R., Propst, J., van Essen, T., Choi, M., Lee, S., Chae, J. H., Price, S., Schnur, R. E., Douglas, G., Wentzensen, I. M., Zweier, C., Reis, A., Bialer, M. G., Moore, C., Koopmans, M., Brilstra, E. H., Monroe, G. R., van Gassen, K. L. I., van Binsbergen, E., Newbury-Ecob, R., Bownass, L., Bader, I., Mayr, J. A., Wortmann, S. B., Jakielski, K. J., Strand, E. A., Kloth, K., Bierhals, T., Roberts, J. D., Petrovich, R. M., Machida, S., Kurumizaka, H., Lelieveld, S., Pfundt, R., Jansen, S., Deriziotis, P., Faivre, L., Thevenon, J., Assoum, M., Shriberg, L., Kleefstra, T., Brunner, H. G., Wade, P. A., Fisher, S. E., & Campeau, P. M. (2019). Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature communications, 10(1), 883. https://doi.org/10.1038/s41467-019-08800-2
Blok, Lot Snijders, et al. "Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language." Nature communications vol. 10,1 (2019): 883. doi: https://doi.org/10.1038/s41467-019-08800-2
Blok LS, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T, Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nat Commun. 2019 Feb 15;10(1):883. doi: 10.1038/s41467-019-08800-2. PMID: 30770872; PMCID: PMC6377600.
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Nat Commun. 2019 Feb 15;10(1):883. doi: 10.1038/s41467-019-08800-2.

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Nature communications

Lot Snijders Blok, Justine Rousseau, Joanna Twist, Sophie Ehresmann, Motoki Takaku, Hanka Venselaar, Lance H Rodan, Catherine B Nowak, Jessica Douglas, Kathryn J Swoboda, Marcie A Steeves, Inderneel Sahai, Connie T R M Stumpel, Alexander P A Stegmann, Patricia Wheeler, Marcia Willing, Elise Fiala, Aaina Kochhar, William T Gibson, Ana S A Cohen, Ruky Agbahovbe, A Micheil Innes, P Y Billie Au, Julia Rankin, Ilse J Anderson, Steven A Skinner, Raymond J Louie, Hannah E Warren, Alexandra Afenjar, Boris Keren, Caroline Nava, Julien Buratti, Arnaud Isapof, Diana Rodriguez, Raymond Lewandowski, Jennifer Propst, Ton van Essen, Murim Choi, Sangmoon Lee, Jong H Chae, Susan Price, Rhonda E Schnur, Ganka Douglas, Ingrid M Wentzensen, Christiane Zweier, André Reis, Martin G Bialer, Christine Moore, Marije Koopmans, Eva H Brilstra, Glen R Monroe, Koen L I van Gassen, Ellen van Binsbergen, Ruth Newbury-Ecob, Lucy Bownass, Ingrid Bader, Johannes A Mayr, Saskia B Wortmann, Kathy J Jakielski, Edythe A Strand, Katja Kloth, Tatjana Bierhals, John D Roberts, Robert M Petrovich, Shinichi Machida, Hitoshi Kurumizaka, Stefan Lelieveld, Rolph Pfundt, Sandra Jansen, Pelagia Deriziotis, Laurence Faivre, Julien Thevenon, Mirna Assoum, Lawrence Shriberg, Tjitske Kleefstra, Han G Brunner, Paul A Wade, Simon E Fisher, Philippe M Campeau

Affiliations

  1. Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.
  2. Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands.
  3. Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands.
  4. CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada.
  5. National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.
  6. Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.
  7. Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.
  8. Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.
  9. Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, 02114, USA.
  10. Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands.
  11. Nemours Childrens Clinic, Orlando, FL, 32827, USA.
  12. Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA.
  13. Valley Children's Hospital, Madera, CA, 93636, USA.
  14. British Columbia Children's Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada.
  15. Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada.
  16. Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, T2N 4N1, Canada.
  17. Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust (Heavitree), Exeter, EX2 5DW, UK.
  18. Division of Genetics, Department of Medicine, University of Tennessee Medical Center, Knoxville, TN, 37920, USA.
  19. Greenwood Genetic Center, Greenwood, SC, 29646, USA.
  20. GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris ; Department of Medical Genetics and Centre de Référence Malformations et maladies congénitales du cervelet et déficiences intellectuelles de causes rares, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France.
  21. AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.
  22. Groupe de Recherche Clinique (GRC) 'déficience intellectuelle et autisme' UPMC, Paris, 75005, France.
  23. INSERM, U 1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, 75013, Paris, France.
  24. GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department Child Neurology and Reference Center for Neuromuscular Diseases "Nord/Est/Ile-de-France", FILNEMUS, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France.
  25. GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department of Child Neurology and National Reference Center for Neurogenetic Disorders, Armand Trousseau Hospital, GHUEP, AP-HP, INSERM U1141, 75012, Paris, France.
  26. Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA, 23298, USA.
  27. Clinical Genetics Department, University Medical Center Groningen, Groningen, 9700RB, The Netherlands.
  28. Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea.
  29. Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Children's Hospital, Seoul, 08826, Republic of Korea.
  30. Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 7HE, UK.
  31. GeneDx, Gaithersburg, MD, 20877, USA.
  32. Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany.
  33. Northwell Health, Division of Medical Genetics and Genomics, Great Neck NY, 11021, USA.
  34. Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.
  35. University Hospitals Bristol, Department of Clinical Genetics, St Michael's Hospital, Bristol, BS2 8EG, UK.
  36. Department of Clinical Genetics, University Children's Hospital, Paracelsus Medical University, Salzburg, A-5020, Austria.
  37. Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, A-5020, Austria.
  38. Institute of Human Genetics, Technische Universität München, Munich, 81675, Germany.
  39. Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, 85764, Germany.
  40. Communication Sciences and Disorders, Augustana College, Rock Island, IL, 61201, USA.
  41. Department of Neurology, Mayo Clinic, Rochester, MN, 55905, USA.
  42. Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany.
  43. Waseda University, Tokyo, 169-8050, Japan.
  44. Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté, Dijon, 21070, France.
  45. Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France.
  46. Waisman Center, Phonology Project, Madison, WI, 53705-2280, USA.
  47. Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands. [email protected].
  48. Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands. [email protected].
  49. CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada. [email protected].
  50. Sainte-Justine Hospital, University of Montreal, Montreal, QC, H3T 1C5, Canada. [email protected].

PMID: 30770872 PMCID: PMC6377600 DOI: 10.1038/s41467-019-08800-2

Abstract

The original version of this Article contained an error in the spelling of the author Laurence Faivre, which was incorrectly given as Laurence Faive. This has now been corrected in both the PDF and HTML versions of the Article.

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