Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis

Karin Weiss¹, Hayley P Lazar², Alina Kurolap^{3

4}, Ariel F Martinez⁵, Tamar Paperna³, Lior Cohen⁶, Marie F Smeland⁷, Sandra Whalen⁸, Solveig Heide⁹, Boris Keren⁹, Pauline Terhal¹⁰, Melita Irving¹¹, Motoki Takaku², John D Roberts², Robert M Petrovich², Samantha A Schrier Vergano^{12

13}, Amy Kenney¹², Hanne Hove¹⁴, Elizabeth DeChene¹⁵, Shane C Quinonez¹⁶, Estelle Colin¹⁷, Alban Ziegler¹⁷, Melissa Rumple¹⁸, Mahim Jain^{5

19}, Danielle Monteil²⁰, Elizabeth R Roeder²¹, Kimberly Nugent²¹, Arie van Haeringen²², Michael Gambello²³, Avni Santani¹⁵, Līvija Medne²⁴, Bryan Krock¹⁵, Cara M Skraban²⁴, Elaine H Zackai²⁴, Holly A Dubbs²⁵, Thomas Smol^{26

27}, Jamal Ghoumid^{26

27}, Michael J Parker²⁸, Michael Wright²⁹, Peter Turnpenny³⁰, Jill Clayton-Smith^{31

32}, Kay Metcalfe^{31

32}, Hitoshi Kurumizaka³³, Bruce D Gelb³⁴, Hagit Baris Feldman^{3

4}, Philippe M Campeau³⁵, Maximilian Muenke⁵, Paul A Wade^#², Katherine Lachlan^#³⁶

Affiliations

¹ The Genetics Institute, Rambam Health Care Campus, Haifa, Israel. k_weiss@rambam.health.gov.il.
² Epigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
³ The Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
⁴ The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
⁵ Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
⁶ Genetics Institute, Schneider Children's Medical Center, Petah Tikva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
⁷ Department of Medical Genetics, University Hospital of North Norway, Tromsø, Norway.
⁸ UF de génétique clinique, Centre de Référence Maladies Rares des Anomalies du développement et syndromes malformatifs, APHP, Hôpital Trousseau, Paris, France.
⁹ AP-HP, Département de Génétique, Centre de Référence Maladies Rares "Anomalies du développement et syndromes malformatifs" Hôpital de la Pitié Salpêtrière, Paris, France.
¹⁰ Department of Genetics, Utrecht University Medical Center, Utrecht, the Netherlands.
¹¹ Department of Clinical Genetics, Guy's Hospital, London, UK.
¹² Division of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, VA, USA.
¹³ Department of Pediatrics, Eastern Virginia Medical School, Norfolk, VA, USA.
¹⁴ Centre for Rare Diseases, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
¹⁵ Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
¹⁶ Department of Pediatrics, Division of Genetics, Metabolism and Genomic Medicine, University of Michigan, Ann Arbor, MI, USA.
¹⁷ Department of Biochemistry and Genetics, University Hospital Angers, Angers, France.
¹⁸ Banner Child Neurology, Glendale, AZ, USA.
¹⁹ Bone and Osteogenesis Imperfecta Department, Kennedy Krieger Institute, Baltimore, MD, USA.
²⁰ Department of Pediatrics, Naval Medical Center Portsmouth, Portsmouth, VA, USA.
²¹ Departments of Pediatrics and Molecular and Human Genetics, Baylor College of Medicine, San Antonio, TX, USA.
²² Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
²³ Department of Human Genetics, School of Medicine, Emory University, Atlanta, GA, USA.
²⁴ Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
²⁵ Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
²⁶ Department of Clinical Genetics, Lille University Hospital, CHU Lille, Lille, France.
²⁷ EA7364 RADEME (Research Team on Rare Developmental and Metabolic Diseases), Lille 2 University, Lille, France.
²⁸ Sheffield Children's Hospital NHS Foundation Trust, Western Bank, Sheffield, UK.
²⁹ Northern Genetics Service, Newcastle Upon Tyne Hospitals NHS Foundation Trust, Institute of Human Genetics, International Centre for Life, Newcastle upon Tyne, UK.
³⁰ University of Exeter Medical School, Clinical Genetics Royal Devon & Exeter Hospital, Exeter, UK.
³¹ Institute of Evolution, Systems and Genomics, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
³² Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre, Manchester, UK.
³³ Laboratory of Structural Biology, Graduate School of Advanced Science & Engineering, Waseda University, Tokyo, Japan.
³⁴ Mindich Child Health and Development Institute and Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
³⁵ Department of Pediatrics, University of Montreal and CHU Sainte-Justine, Montreal, QC, Canada.
³⁶ Wessex Clinical Genetics Service, University Hospital Southampton NHS Trust. Department of Human Genetics and Genomic Medicine, Southampton University, Southampton, UK.

^# Contributed equally.

PMID: 31844176
DOI: 10.1038/s41436-019-0727-3

Free article

Published Erratum

Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis

Karin Weiss et al. Genet Med. 2020 Mar.

Free article

. 2020 Mar;22(3):669.

doi: 10.1038/s41436-019-0727-3.

Authors

Affiliations

¹ The Genetics Institute, Rambam Health Care Campus, Haifa, Israel. k_weiss@rambam.health.gov.il.
² Epigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
³ The Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
⁴ The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
⁵ Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
⁶ Genetics Institute, Schneider Children's Medical Center, Petah Tikva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
⁷ Department of Medical Genetics, University Hospital of North Norway, Tromsø, Norway.
⁸ UF de génétique clinique, Centre de Référence Maladies Rares des Anomalies du développement et syndromes malformatifs, APHP, Hôpital Trousseau, Paris, France.
⁹ AP-HP, Département de Génétique, Centre de Référence Maladies Rares "Anomalies du développement et syndromes malformatifs" Hôpital de la Pitié Salpêtrière, Paris, France.
¹⁰ Department of Genetics, Utrecht University Medical Center, Utrecht, the Netherlands.
¹¹ Department of Clinical Genetics, Guy's Hospital, London, UK.
¹² Division of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, VA, USA.
¹³ Department of Pediatrics, Eastern Virginia Medical School, Norfolk, VA, USA.
¹⁴ Centre for Rare Diseases, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
¹⁵ Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
¹⁶ Department of Pediatrics, Division of Genetics, Metabolism and Genomic Medicine, University of Michigan, Ann Arbor, MI, USA.
¹⁷ Department of Biochemistry and Genetics, University Hospital Angers, Angers, France.
¹⁸ Banner Child Neurology, Glendale, AZ, USA.
¹⁹ Bone and Osteogenesis Imperfecta Department, Kennedy Krieger Institute, Baltimore, MD, USA.
²⁰ Department of Pediatrics, Naval Medical Center Portsmouth, Portsmouth, VA, USA.
²¹ Departments of Pediatrics and Molecular and Human Genetics, Baylor College of Medicine, San Antonio, TX, USA.
²² Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
²³ Department of Human Genetics, School of Medicine, Emory University, Atlanta, GA, USA.
²⁴ Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
²⁵ Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
²⁶ Department of Clinical Genetics, Lille University Hospital, CHU Lille, Lille, France.
²⁷ EA7364 RADEME (Research Team on Rare Developmental and Metabolic Diseases), Lille 2 University, Lille, France.
²⁸ Sheffield Children's Hospital NHS Foundation Trust, Western Bank, Sheffield, UK.
²⁹ Northern Genetics Service, Newcastle Upon Tyne Hospitals NHS Foundation Trust, Institute of Human Genetics, International Centre for Life, Newcastle upon Tyne, UK.
³⁰ University of Exeter Medical School, Clinical Genetics Royal Devon & Exeter Hospital, Exeter, UK.
³¹ Institute of Evolution, Systems and Genomics, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
³² Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre, Manchester, UK.
³³ Laboratory of Structural Biology, Graduate School of Advanced Science & Engineering, Waseda University, Tokyo, Japan.
³⁴ Mindich Child Health and Development Institute and Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
³⁵ Department of Pediatrics, University of Montreal and CHU Sainte-Justine, Montreal, QC, Canada.
³⁶ Wessex Clinical Genetics Service, University Hospital Southampton NHS Trust. Department of Human Genetics and Genomic Medicine, Southampton University, Southampton, UK.

^# Contributed equally.

PMID: 31844176
DOI: 10.1038/s41436-019-0727-3

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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Erratum for

The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Weiss K, Lazar HP, Kurolap A, Martinez AF, Paperna T, Cohen L, Smeland MF, Whalen S, Heide S, Keren B, Terhal P, Irving M, Takaku M, Roberts JD, Petrovich RM, Schrier Vergano SA, Kenney A, Hove H, DeChene E, Quinonez SC, Colin E, Ziegler A, Rumple M, Jain M, Monteil D, Roeder ER, Nugent K, van Haeringen A, Gambello M, Santani A, Medne L, Krock B, Skraban CM, Zackai EH, Dubbs HA, Smol T, Ghoumid J, Parker MJ, Wright M, Turnpenny P, Clayton-Smith J, Metcalfe K, Kurumizaka H, Gelb BD, Baris Feldman H, Campeau PM, Muenke M, Wade PA, Lachlan K. Weiss K, et al. Genet Med. 2020 Feb;22(2):389-397. doi: 10.1038/s41436-019-0612-0. Epub 2019 Aug 7. Genet Med. 2020. PMID: 31388190 Free PMC article.

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Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis

Affiliations

Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis

Authors

Affiliations

Abstract

Erratum for

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LinkOut - more resources

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