Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant

Beauregard-Lacroix, Eliane; Pacheco-Cuellar, Guillermo; Ajeawung, Norbert F.; Tardif, Jessica; Dieterich, Klaus; Dabir, Tabib; Vind-Kezunovic, Dina; White, Susan M.; Zadori, Denes; Castiglioni, Claudia; Tranebjærg, Lisbeth; Tørring, Pernille Mathiesen; Blair, Ed; Wisniewska, Marzena; Camurri, Maria Vittoria; van Bever, Yolande; Molidperee, Sirinart; Taylor, Juliet; Dionne-Laporte, Alexandre; Sisodiya, Sanjay M.; Hennekam, Raoul C. M.; Campeau, Philippe M.

doi:10.1038/s41436-020-00969-y

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Correction
Published: 15 September 2020

Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant

Eliane Beauregard-Lacroix MD¹,
Guillermo Pacheco-Cuellar MD, MSc¹,
Norbert F. Ajeawung PhD²,
Jessica Tardif MSc¹,
Klaus Dieterich MD, PhD ORCID: orcid.org/0000-0002-4362-4062³,
Tabib Dabir MD, DCH⁴,
Dina Vind-Kezunovic MD, PhD⁵,
Susan M. White MBBS⁶,
Denes Zadori MD, PhD⁷,
Claudia Castiglioni MD⁸,
Lisbeth Tranebjærg MD, PhD^9,10,
Pernille Mathiesen Tørring MD, PhD¹¹,
Ed Blair BMSc(Hons), MBchB¹²,
Marzena Wisniewska MD¹³,
Maria Vittoria Camurri MSc¹,
Yolande van Bever MD¹⁴,
Sirinart Molidperee BSc²,
Juliet Taylor MBChB¹⁵,
Alexandre Dionne-Laporte MSc¹⁶,
Sanjay M. Sisodiya MD^17,18,
Raoul C. M. Hennekam MD, PhD¹⁹ &
…
Philippe M. Campeau MD ORCID: orcid.org/0000-0001-9713-7107¹

Genetics in Medicine volume 23, page 237 (2021)Cite this article

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The Original Article was published on 02 September 2020

Correction to: Genetics in Medicine 2020; https://doi.org/10.1038/s41436-020-00950-9, published online 02 September 2020

In the original version of this Article, the affiliation details for Guillermo Pacheco-Cuellar, Jessica Tardif, Maria Vittoria Camurri, Sirinart Molidperee, and Philippe M. Campeau were incorrectly given. They have now been corrected in both the PDF and HTML versions of the Article.

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Authors and Affiliations

Medical Genetics Division, Department of Pediatrics, Sainte-Justine University Hospital Center, Montreal, QC, Canada
Eliane Beauregard-Lacroix MD, Guillermo Pacheco-Cuellar MD, MSc, Jessica Tardif MSc, Maria Vittoria Camurri MSc & Philippe M. Campeau MD
CHU Sainte Justine Research Center, Université de Montréal, Montreal, QC, Canada
Norbert F. Ajeawung PhD & Sirinart Molidperee BSc
Univ. Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences (GIN), Grenoble, France
Klaus Dieterich MD, PhD
Department of Genetic Medicine, Belfast City Hospital, Belfast, Northern Ireland, UK
Tabib Dabir MD, DCH
Department of Dermatology, Copenhagen University Hospital Bispebjerg, Copenhagen, NV, Denmark
Dina Vind-Kezunovic MD, PhD
Victorian Clinical Genetics Services, Murdoch Children’s Research Institute, Melbourne, Australia
Susan M. White MBBS
Department of Neurology, Interdisciplinary Excellence Center, Faculty of Medicine, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, Hungary
Denes Zadori MD, PhD
Department of Pediatric Neurology, Clínica Las Condes, Santiago, Chile
Claudia Castiglioni MD
The Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
Lisbeth Tranebjærg MD, PhD
Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
Lisbeth Tranebjærg MD, PhD
Department of Clinical Genetics, Odense University Hospital, Odense, Denmark
Pernille Mathiesen Tørring MD, PhD
Oxford Regional Genetics Service, Oxford University Hospitals, Oxford, UK
Ed Blair BMSc(Hons), MBchB
Department of Medical Genetics, Poznañ University of Medical Sciences, Poznañ, Poland
Marzena Wisniewska MD
Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands
Yolande van Bever MD
Genetic Health Service New Zealand–Northern Hub, Auckland, New Zealand
Juliet Taylor MBChB
Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, QC, Canada
Alexandre Dionne-Laporte MSc
Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK
Sanjay M. Sisodiya MD
Chalfont Centre for Epilepsy, Bucks, UK
Sanjay M. Sisodiya MD
Department of Pediatrics, Amsterdam University Medical Center, Amsterdam, Netherlands
Raoul C. M. Hennekam MD, PhD

Authors

Eliane Beauregard-Lacroix MD
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Guillermo Pacheco-Cuellar MD, MSc
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Norbert F. Ajeawung PhD
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Jessica Tardif MSc
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Klaus Dieterich MD, PhD
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Tabib Dabir MD, DCH
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Dina Vind-Kezunovic MD, PhD
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Susan M. White MBBS
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Denes Zadori MD, PhD
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Claudia Castiglioni MD
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Lisbeth Tranebjærg MD, PhD
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Pernille Mathiesen Tørring MD, PhD
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Ed Blair BMSc(Hons), MBchB
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Marzena Wisniewska MD
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Maria Vittoria Camurri MSc
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Yolande van Bever MD
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Sirinart Molidperee BSc
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Juliet Taylor MBChB
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Alexandre Dionne-Laporte MSc
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Sanjay M. Sisodiya MD
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Raoul C. M. Hennekam MD, PhD
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Philippe M. Campeau MD
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Corresponding author

Correspondence to Philippe M. Campeau MD.

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Beauregard-Lacroix, E., Pacheco-Cuellar, G., Ajeawung, N.F. et al. Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant. Genet Med 23, 237 (2021). https://doi.org/10.1038/s41436-020-00969-y

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Published: 15 September 2020
Issue Date: January 2021
DOI: https://doi.org/10.1038/s41436-020-00969-y

Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant

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