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

Sahar Elouej¹, Karim Harhouri¹, Morgane Le Mao², Genevieve Baujat³, Sheela Nampoothiri⁴, Hϋlya Kayserili⁵, Nihal Al Menabawy⁶, Laila Selim⁶, Arianne Llamos Paneque⁷, Christian Kubisch⁸, Davor Lessel⁸, Robert Rubinsztajn⁹, Chayki Charar¹⁰, Catherine Bartoli¹, Coraline Airault¹, Jean-François Deleuze¹¹, Agnes Rötig¹², Peter Bauer¹³, Catarina Pereira¹³, Abigail Loh¹⁴, Nathalie Escande-Beillard^{5

14}, Antoine Muchir¹⁵, Lisa Martino¹⁶, Yosef Gruenbaum¹⁰, Song-Hua Lee¹⁶, Philippe Manivet^{16

17

18}, Guy Lenaers², Bruno Reversade^{5

14}, Nicolas Lévy^{1

19}, Annachiara De Sandre-Giovannoli^{20

21

22}

Affiliations

¹ Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.
² MitoLab, Mitochondrial Medicine Research Centre, Institut MITOVASC, CNRS UMR 6015, INSERM U1083, Université d'Angers, CHU d'Angers, Angers, France.
³ Department of Medical Genetics, INSERM UMR 1163, Paris Descartes-Sorbonne Paris Cité University, IMAGINE Institute, Necker Enfants Malades Hospital, Paris, France.
⁴ Department of Pediatric Genetics, Amrita Institute of Medical Sciences & Research Centre, AIMS Ponekkara PO Cochin, Kerala, India.
⁵ Medical Genetics Department, Koç University, School of Medicine (KUSoM), Istanbul, Turkey.
⁶ Neurology and Metabolic Division, Cairo University Children Hospital, Cairo, Egypt.
⁷ Medical Genetics Service Specialties Hospital FF AA No.1, Quito, Ecuador.
⁸ Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
⁹ Pole of Anesthesiology and Reanimation, , Necker Enfants Malades Hospital, Paris, France.
¹⁰ Department of Genetics, Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
¹¹ Centre National de Recherche en Génomique Humaine (CNRGH) and Centre d'Etude du Polymorphisme Humain (CEPH), Institut de Biologie François Jacob, CEA, Université Paris-Saclay and Fondation Jean Dausset, Paris, France.
¹² INSERM UMR1163, Institut Imagine, Paris, France.
¹³ CENTOGENE AG, Rostock, Germany.
¹⁴ Institute of Medical Biology, A*STAR, Singapore, Singapore.
¹⁵ Sorbonne Université, INSERM, Institute of Myology, Center of Research in Myology, Paris, France.
¹⁶ CeleScreen SAS, Paris, France.
¹⁷ APHP, Biobank Lariboisière BB-0033-00064, Platform of BioPathology and Innovative Technologies in Health, Hôpital Lariboisière, Paris, France.
¹⁸ INSERM UMR1141 « NeuroDiderot », Université de Paris, Paris, France.
¹⁹ Department of Medical Genetics, La Timone Children's Hospital, Marseille, France.
²⁰ Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France. annachiara.desandre-giovannoli@univ-amu.fr.
²¹ Department of Medical Genetics, La Timone Children's Hospital, Marseille, France. annachiara.desandre-giovannoli@univ-amu.fr.
²² Biological Resource Center (CRB-TAC), Assistance Publique Hôpitaux de Marseille, La Timone Children's Hospital, Marseille, France. annachiara.desandre-giovannoli@univ-amu.fr.

PMID: 33077719
PMCID: PMC7572408
DOI: 10.1038/s41467-020-19290-y

Published Erratum

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

Sahar Elouej et al. Nat Commun. 2020.

. 2020 Oct 19;11(1):5349.

doi: 10.1038/s41467-020-19290-y.

Authors

Affiliations

¹ Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.
² MitoLab, Mitochondrial Medicine Research Centre, Institut MITOVASC, CNRS UMR 6015, INSERM U1083, Université d'Angers, CHU d'Angers, Angers, France.
³ Department of Medical Genetics, INSERM UMR 1163, Paris Descartes-Sorbonne Paris Cité University, IMAGINE Institute, Necker Enfants Malades Hospital, Paris, France.
⁴ Department of Pediatric Genetics, Amrita Institute of Medical Sciences & Research Centre, AIMS Ponekkara PO Cochin, Kerala, India.
⁵ Medical Genetics Department, Koç University, School of Medicine (KUSoM), Istanbul, Turkey.
⁶ Neurology and Metabolic Division, Cairo University Children Hospital, Cairo, Egypt.
⁷ Medical Genetics Service Specialties Hospital FF AA No.1, Quito, Ecuador.
⁸ Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
⁹ Pole of Anesthesiology and Reanimation, , Necker Enfants Malades Hospital, Paris, France.
¹⁰ Department of Genetics, Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
¹¹ Centre National de Recherche en Génomique Humaine (CNRGH) and Centre d'Etude du Polymorphisme Humain (CEPH), Institut de Biologie François Jacob, CEA, Université Paris-Saclay and Fondation Jean Dausset, Paris, France.
¹² INSERM UMR1163, Institut Imagine, Paris, France.
¹³ CENTOGENE AG, Rostock, Germany.
¹⁴ Institute of Medical Biology, A*STAR, Singapore, Singapore.
¹⁵ Sorbonne Université, INSERM, Institute of Myology, Center of Research in Myology, Paris, France.
¹⁶ CeleScreen SAS, Paris, France.
¹⁷ APHP, Biobank Lariboisière BB-0033-00064, Platform of BioPathology and Innovative Technologies in Health, Hôpital Lariboisière, Paris, France.
¹⁸ INSERM UMR1141 « NeuroDiderot », Université de Paris, Paris, France.
¹⁹ Department of Medical Genetics, La Timone Children's Hospital, Marseille, France.
²⁰ Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France. annachiara.desandre-giovannoli@univ-amu.fr.
²¹ Department of Medical Genetics, La Timone Children's Hospital, Marseille, France. annachiara.desandre-giovannoli@univ-amu.fr.
²² Biological Resource Center (CRB-TAC), Assistance Publique Hôpitaux de Marseille, La Timone Children's Hospital, Marseille, France. annachiara.desandre-giovannoli@univ-amu.fr.

PMID: 33077719
PMCID: PMC7572408
DOI: 10.1038/s41467-020-19290-y

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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Erratum for

Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.
Elouej S, Harhouri K, Le Mao M, Baujat G, Nampoothiri S, Kayserili H, Menabawy NA, Selim L, Paneque AL, Kubisch C, Lessel D, Rubinsztajn R, Charar C, Bartoli C, Airault C, Deleuze JF, Rötig A, Bauer P, Pereira C, Loh A, Escande-Beillard N, Muchir A, Martino L, Gruenbaum Y, Lee SH, Manivet P, Lenaers G, Reversade B, Lévy N, De Sandre-Giovannoli A. Elouej S, et al. Nat Commun. 2020 Sep 11;11(1):4589. doi: 10.1038/s41467-020-18146-9. Nat Commun. 2020. PMID: 32917887 Free PMC article.

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

Affiliations

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

Authors

Affiliations

Abstract

Erratum for

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