Correction to: Nature Genetics https://doi.org/10.1038/s41588-021-00970-4, published online 13 December 2021.
In the version of this article initially published, CIROP was defined as ciliated left–right organizer metallopeptide instead of ciliated left–right organizer metallopeptidase. Also, accession codes for the human CIROP cDNA (NM_001402427.1) and protein (NP_001389356.1) reference sequences have been added. In Fig. 1 and the text, MIM numbers were inserted that are now available for CIROP and C1orf127 genes, as well as for the disorder caused by CIROP mutations (HTX12). Finally, in the section ‘CIROP is mutated in human patients with recessive HTX’, the mutation p.Cys269Ser was incorrectly shown as in ‘p.Cys296Ser’. The amendments have been made in the HTML and PDF versions of the article.
Author information
Yan Ling Chong
Present address: Department of Pathology, National University Hospital, Singapore, Singapore
Guillaume Louvel
Present address: Écologie, Systématique et Évolution, UMR 8079 CNRS – Université Paris-Saclay – AgroParisTech, Orsay, France
Priyanka Anujan
Present address: Institute of Reproductive and Developmental Biology, Hammersmith Hospital, Imperial College, London, UK
Chun Teck Lim
Present address: Singapore Institute of Food and Biotechnology Innovation (SIFBI), A*STAR, Singapore, Singapore
These authors contributed equally: Emmanuelle Szenker-Ravi, Tim Ott.
Authors and Affiliations
Laboratory of Human Genetics and Therapeutics, Genome Institute of Singapore (GIS), A*STAR, Singapore, Singapore
Emmanuelle Szenker-Ravi, Muznah Khatoo, Wei Xuan Goh, Darshini Kannesan & Bruno Reversade
Institute of Biology, University of Hohenheim, Stuttgart, Germany
Tim Ott & Martin Blum
Laboratoire de Cardiogénétique, Groupe Hospitalier Est, Hospices Civils de Lyon, Lyon, France
Anne Moreau de Bellaing
Institute of Molecular and Cell Biology (IMCB), A*STAR, Singapore, Singapore
Yan Ling Chong, Priyanka Anujan, Vydianathan Ravi, Sumanty Tohari, Byrappa Venkatesh, Sudipto Roy & Bruno Reversade
Institute for Molecular Biology, Hannover Medical School, Hannover, Germany
Anja Beckers & Achim Gossler
REBIRTH Cluster of Excellence, Hannover, Germany
Anja Beckers & Achim Gossler
Institut de Biologie de l’Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, PSL Research University, Paris, France
Guillaume Louvel & Hugues Roest Crollius
Skin Research Institute of Singapore (SRIS), A*STAR, Singapore, Singapore
Carine Bonnard
CPDPN, Pôle mère enfant, Maison de Santé Protestante Bordeaux Bagatelle, Talence, France
Sébastien Moutton
Praxis Dr Patric SCHÖN, Oberschleissheim, Germany
Patric Schoen
Service de Génétique Médicale, Hôpital Sud, CHU de Rennes, Rennes, France
Mélanie Fradin
Service de Génétique Médicale, CHU d’Angers, Angers, France
Estelle Colin
Department of Human Genetics, Gilbert and Rose-Marie Chagoury School of Medicine, Lebanese American University, Beirut, Lebanon
André Megarbane
Institut Jérôme LEJEUNE, Paris, France
André Megarbane
Department of Pediatric Cardiology, Hôtel Dieu de France University Medical Center, Saint Joseph University, Alfred Naccache Boulevard, Achrafieh, Beirut, Lebanon
Linda Daou & Ghassan Chehab
Department of Pediatrics, Lebanese University, Faculty of Medical Sciences, Hadath, Greater Beirut, Lebanon
Ghassan Chehab
Service de Cardiologie Pédiatrique, Groupe Hospitalier Est, Hospices Civils de Lyon, Bron, France
Sylvie Di Filippo
Service de Génétique, University of Bordeaux, MRGM, INSERM U1211, CHU de Bordeaux, Bordeaux, France
Caroline Rooryck
Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), Evry, France
Jean-François Deleuze & Anne Boland
Service de Cardiologie Pédiatrique, Hôpital Universitaire des Enfants Reine Fabiola (HUDERF), Brussels, Belgium
Nicolas Arribard
Pediatrics Department, Pediatric Cardiology Division, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey
Rukiye Eker
Molecular Diagnosis Centre (MDC), National University Hospital (NUH), Singapore, Singapore
Alvin Yu-Jin Ng
Fédération de Génétique, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris, Paris, France
Marlène Rio, Jeanne Amiel & Tania Attie-Bitach
Developmental Brain Disorders Laboratory, Université de Paris, Imagine Institute, INSERM UMR 1163, Paris, France
Marlène Rio
Bioinformatics Institute (BII), A*STAR, Singapore, Singapore
Chun Teck Lim, Birgit Eisenhaber & Frank Eisenhaber
Genome Institute of Singapore (GIS), A*STAR, Singapore, Singapore
Birgit Eisenhaber & Frank Eisenhaber
School of Biological Sciences (SBS), Nanyang Technological University (NTU), Singapore, Singapore
Frank Eisenhaber
Department of Pediatrics, National University of Singapore (NUS), Singapore, Singapore
Byrappa Venkatesh, Sudipto Roy & Bruno Reversade
Laboratory of Embryology and Genetics of Malformations, Université de Paris, Imagine Institute, INSERM UMR 1163, Paris, France
Jeanne Amiel & Christopher T. Gordon
Department of Biological Sciences, National University of Singapore (NUS), Singapore, Singapore
Sudipto Roy
Laboratory of Genetics and Development of the Cerebral Cortex, Université de Paris, Imagine Institute, INSERM UMR 1163, Paris, France
Tania Attie-Bitach
CPDPN, Hôpital MFME, CHU de Martinique, Fort de France, France
Patrice Bouvagnet
Medical Genetics Department, Koç University School of Medicine (KUSOM), Istanbul, Turkey
Bruno Reversade
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Szenker-Ravi, E., Ott, T., Khatoo, M. et al. Publisher Correction: Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates. Nat Genet 54, 906 (2022). https://doi.org/10.1038/s41588-022-01053-8
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DOI: https://doi.org/10.1038/s41588-022-01053-8
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