Correction: Long-read trio sequencing of individuals with unsolved intellectual disability

Pauper, Marc; Kucuk, Erdi; Wenger, Aaron M.; Chakraborty, Shreyasee; Baybayan, Primo; Kwint, Michael; van der Sanden, Bart; Nelen, Marcel R.; Derks, Ronny; Brunner, Han G.; Hoischen, Alexander; Vissers, Lisenka E. L. M.; Gilissen, Christian

doi:10.1038/s41431-021-00868-z

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Correction
Published: 26 March 2021

Correction: Long-read trio sequencing of individuals with unsolved intellectual disability

Marc Pauper¹^na1,
Erdi Kucuk ORCID: orcid.org/0000-0002-3970-7068^1,2^na1,
Aaron M. Wenger³,
Shreyasee Chakraborty³,
Primo Baybayan³,
Michael Kwint¹,
Bart van der Sanden ORCID: orcid.org/0000-0003-0546-1351^1,4,
Marcel R. Nelen¹,
Ronny Derks¹,
Han G. Brunner^1,2,5,
Alexander Hoischen^1,2,6^na1,
Lisenka E. L. M. Vissers ORCID: orcid.org/0000-0001-6470-5497^1,4^na1 &
…
Christian Gilissen ORCID: orcid.org/0000-0003-1693-9699^1,2^na1

European Journal of Human Genetics volume 29, page 720 (2021)Cite this article

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The Original Article was published on 30 November 2020

Correction to: Eur J Hum Genet

https://doi.org/10.1038/s41431-020-00770-0

The authors inadvertently included tracked changes in their Supplemental Material file in error. These have been now been removed.

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These authors contributed equally: Marc Pauper, Erdi Kucuk, Alexander Hoischen, Lisenka E. L. M. Vissers, Christian Gilissen

Authors and Affiliations

Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands
Marc Pauper, Erdi Kucuk, Michael Kwint, Bart van der Sanden, Marcel R. Nelen, Ronny Derks, Han G. Brunner, Alexander Hoischen, Lisenka E. L. M. Vissers & Christian Gilissen
Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen, The Netherlands
Erdi Kucuk, Han G. Brunner, Alexander Hoischen & Christian Gilissen
Pacific Biosciences, Menlo Park, CA, USA
Aaron M. Wenger, Shreyasee Chakraborty & Primo Baybayan
Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands
Bart van der Sanden & Lisenka E. L. M. Vissers
Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands
Han G. Brunner
Department of Internal Medicine, Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, The Netherlands
Alexander Hoischen

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Marc Pauper
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Erdi Kucuk
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Primo Baybayan
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Michael Kwint
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Marcel R. Nelen
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Ronny Derks
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Alexander Hoischen
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Lisenka E. L. M. Vissers
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Christian Gilissen
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Correspondence to Christian Gilissen.

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Pauper, M., Kucuk, E., Wenger, A.M. et al. Correction: Long-read trio sequencing of individuals with unsolved intellectual disability. Eur J Hum Genet 29, 720 (2021). https://doi.org/10.1038/s41431-021-00868-z

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Published: 26 March 2021
Issue Date: April 2021
DOI: https://doi.org/10.1038/s41431-021-00868-z

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Correction: Long-read trio sequencing of individuals with unsolved intellectual disability

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Copy number variants from 4800 exomes contribute to ~7% of genetic diagnoses in movement disorders, muscle disorders and neuropathies

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Copy number variants from 4800 exomes contribute to ~7% of genetic diagnoses in movement disorders, muscle disorders and neuropathies

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