Correction to: npj Genomic Medicine https://doi.org/10.1038/s41525-022-00308-x, published online 17 June 2022
In the Acknowledgements section, the below content was missing:
“This research has been supported (not financially) by European Reference Network for rare malformation syndromes and rare intellectual and neurodevelopmental disorders, ERN-ITHACA [EU Framework Partnership Agreement ID: 3HP-HP-FPA ERN-01-2016/739516]. This ERN is partly co-funded by the European Union within the framework of the Third Health Programme “ERN- 2016 - Framework Partnership Agreement 2017-2021”.
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Giannuzzi, G., Chatron, N., Mannik, K. et al. Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts. npj Genom. Med. 8, 9 (2023). https://doi.org/10.1038/s41525-023-00354-z
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DOI: https://doi.org/10.1038/s41525-023-00354-z
