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. 2020 Oct 19;11:5349. doi: 10.1038/s41467-020-19290-y

Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology

Sahar Elouej 1,#, Karim Harhouri 1,#, Morgane Le Mao 2, Genevieve Baujat 3, Sheela Nampoothiri 4, Hϋlya Kayserili 5, Nihal Al Menabawy 6, Laila Selim 6, Arianne Llamos Paneque 7, Christian Kubisch 8, Davor Lessel 8, Robert Rubinsztajn 9, Chayki Charar 10, Catherine Bartoli 1, Coraline Airault 1, Jean-François Deleuze 11, Agnes Rötig 12, Peter Bauer 13, Catarina Pereira 13, Abigail Loh 14, Nathalie Escande-Beillard 5,14, Antoine Muchir 15, Lisa Martino 16, Yosef Gruenbaum 10, Song-Hua Lee 16, Philippe Manivet 16,17,18, Guy Lenaers 2, Bruno Reversade 5,14, Nicolas Lévy 1,19, Annachiara De Sandre-Giovannoli 1,19,20,✉
PMCID: PMC7572408  PMID: 33077719

Correction to: Nature Communications 10.1038/s41467-020-18146-9, published online 11 September 2020

The original version of this Article contained errors in the author affiliations.

The affiliations of Nathalie Escande-Beillard and Bruno Reversade with ‘Medical Genetics Department, Koç University, School of Medicine (KUSoM), Istanbul, Turkey’ were inadvertently omitted.

This has now been corrected in both the PDF and HTML versions of the Article.

Articles from Nature Communications are provided here courtesy of Nature Publishing Group

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