Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy

NPJ Genom Med. 2019 May 31:4:11. doi: 10.1038/s41525-019-0086-7. eCollection 2019.

Mark A Corbett¹, Clare L van Eyk¹, Dani L Webber¹, Stephen J Bent², Morgan Newman³, Kelly Harper¹, Jesia G Berry¹, Dimitar N Azmanov⁴, Karen J Woodward^{4

5}, Alison E Gardner¹, Jennie Slee⁶, Luís A Pérez-Jurado^{7

8

9

10}, Alastair H MacLennan¹, Jozef Gecz^{1

10}

¹ 1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
² Data61, Commonwealth Scientific and Industrial Research Organisation, Ecosciences Precinct, Dutton Park, Brisbane, QLD 4102 Australia.
³ 3School of Biological Sciences, University of Adelaide, Adelaide, South Australia 5005 Australia.
⁴ 4Department of Diagnostic Genomics, Queen Elizabeth II Medical Centre, PathWest, Nedlands, WA 6009 Australia.
⁵ 5School of Biomedical Sciences, University of Western Australia, Perth, WA 6009 Australia.
⁶ 6Genetic Services of Western Australia, King Edward Memorial Hospital, Subiaco, WA 6008 Australia.
⁷ 7Genetics Unit, Universitat Pompeu Fabra, Barcelona, 08003 Spain.
⁸ Hospital del Mar Research Institute (IMIM) and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, 08003 Spain.
⁹ 9SA Clinical Genetics, Women's and Children's Hospital & University of Adelaide, Adelaide, South Australia 5006 Australia.
¹⁰ 10South Australian Health and Medical Research Institute, Adelaide, South Australia 5000 Australia.

Abstract

[This corrects the article DOI: 10.1038/s41525-018-0073-4.].

Keywords: Gene expression; Neurodevelopmental disorders; Next-generation sequencing; Structural variation.