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

Author

Listed:
  • Sahar Elouej

    (Aix Marseille Univ, INSERM, MMG)

  • Karim Harhouri

    (Aix Marseille Univ, INSERM, MMG)

  • Morgane Le Mao

    (Institut MITOVASC, CNRS UMR 6015, INSERM U1083, Université d’Angers, CHU d’Angers)

  • Genevieve Baujat

    (Paris Descartes-Sorbonne Paris Cité University, IMAGINE Institute, Necker Enfants Malades Hospital)

  • Sheela Nampoothiri

    (Amrita Institute of Medical Sciences & Research Centre, AIMS Ponekkara PO Cochin)

  • Hϋlya Kayserili

    (Koç University, School of Medicine (KUSoM))

  • Nihal Al Menabawy

    (Cairo University Children Hospital)

  • Laila Selim

    (Cairo University Children Hospital)

  • Arianne Llamos Paneque

    (Medical Genetics Service Specialties Hospital FF AA No.1)

  • Christian Kubisch

    (University Medical Center Hamburg-Eppendorf)

  • Davor Lessel

    (University Medical Center Hamburg-Eppendorf)

  • Robert Rubinsztajn

    (, Necker Enfants Malades Hospital)

  • Chayki Charar

    (Hebrew University of Jerusalem)

  • Catherine Bartoli

    (Aix Marseille Univ, INSERM, MMG)

  • Coraline Airault

    (Aix Marseille Univ, INSERM, MMG)

  • Jean-François Deleuze

    (Université Paris-Saclay and Fondation Jean Dausset)

  • Agnes Rötig

    (Institut Imagine)

  • Peter Bauer

    (CENTOGENE AG)

  • Catarina Pereira

    (CENTOGENE AG)

  • Abigail Loh

    (A*STAR)

  • Nathalie Escande-Beillard

    (Koç University, School of Medicine (KUSoM)
    A*STAR)

  • Antoine Muchir

    (Sorbonne Université, INSERM, Institute of Myology, Center of Research in Myology)

  • Lisa Martino

    (CeleScreen SAS)

  • Yosef Gruenbaum

    (Hebrew University of Jerusalem)

  • Song-Hua Lee

    (CeleScreen SAS)

  • Philippe Manivet

    (CeleScreen SAS
    Platform of BioPathology and Innovative Technologies in Health, Hôpital Lariboisière
    INSERM UMR1141 « NeuroDiderot », Université de Paris)

  • Guy Lenaers

    (Institut MITOVASC, CNRS UMR 6015, INSERM U1083, Université d’Angers, CHU d’Angers)

  • Bruno Reversade

    (Koç University, School of Medicine (KUSoM)
    A*STAR)

  • Nicolas Lévy

    (Aix Marseille Univ, INSERM, MMG
    La Timone Children’s Hospital)

  • Annachiara Sandre-Giovannoli

    (Aix Marseille Univ, INSERM, MMG
    La Timone Children’s Hospital
    Assistance Publique Hôpitaux de Marseille, La Timone Children’s Hospital)

Abstract

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

Suggested Citation

  • Sahar Elouej & Karim Harhouri & Morgane Le Mao & Genevieve Baujat & Sheela Nampoothiri & Hϋlya Kayserili & Nihal Al Menabawy & Laila Selim & Arianne Llamos Paneque & Christian Kubisch & Davor Lessel &, 2020. "Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology," Nature Communications, Nature, vol. 11(1), pages 1-1, December.
    • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-19290-y
    DOI: 10.1038/s41467-020-19290-y
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    Cited by:

    1. Janne Purhonen & Rishi Banerjee & Vilma Wanne & Nina Sipari & Matthias Mörgelin & Vineta Fellman & Jukka Kallijärvi, 2023. "Mitochondrial complex III deficiency drives c-MYC overexpression and illicit cell cycle entry leading to senescence and segmental progeria," Nature Communications, Nature, vol. 14(1), pages 1-23, December.

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