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. 2023 May 24;8:9. doi: 10.1038/s41525-023-00354-z

Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts

Giuliana Giannuzzi 1,2,✉, Nicolas Chatron 1,3,4, Katrin Mannik 1,25, Chiara Auwerx 1,5,6,7, Sylvain Pradervand 1, Gilles Willemin 1, Kendra Hoekzema 8, Xander Nuttle 9,10,11, Jacqueline Chrast 1, Marie C Sadler 5,6,7, Eleonora Porcu 1,6,7; 16p11.2 Consortium, Yann Herault 12, Bertrand Isidor 13, Brigitte Gilbert-Dussardier 14, Evan E Eichler 8,15, Zoltan Kutalik 5,6,7, Alexandre Reymond 1
PMCID: PMC10209113  PMID: 37225732

Correction to: npj Genomic Medicine 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”.

The original article has been corrected.

Contributor Information

Giuliana Giannuzzi, Email: giuliana.giannuzzi@unimi.it.

16p11.2 Consortium:

Katrin Männik, Damien Sanlaville, Caroline Schluth-Bolard, Cédric Le Caignec, Mathilde Nizon, Sandra Martin, Sébastien Jacquemont, Armand Bottani, Marion Gérard, Sacha Weber, Aurélia Jacquette, Catherine Vincent-Delorme, Aurora Currò, Francesca Mari, Alessandra Renieri, Alfredo Brusco, and Giovanni Battista Ferrero


Articles from NPJ Genomic Medicine are provided here courtesy of Nature Publishing Group

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