Published October 19, 2020 | Version v1
Publication Open

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

Creators

  • 1. Inserm
  • 2. Aix-Marseille University
  • 3. Université d'Angers
  • 4. French National Centre for Scientific Research
  • 5. Délégation Paris 5
  • 6. Sorbonne Paris Cité
  • 7. Université Paris Cité
  • 8. Amrita Institute of Medical Sciences and Research Centre
  • 9. Koç University
  • 10. Cairo University
  • 11. Medical Genetics Center
  • 12. University Medical Center Hamburg-Eppendorf
  • 13. Universität Hamburg
  • 14. Hebrew University of Jerusalem
  • 15. Fondation Jean Dausset-CEPH
  • 16. National Center of Human Genomics Research
  • 17. University of Paris-Saclay
  • 18. Atomic Energy and Alternative Energies Commission
  • 19. CEA Saclay
  • 20. Imagine Institute for Genetic Diseases
  • 21. Centogene (Germany)
  • 22. Institute of Medical Biology
  • 23. Agency for Science, Technology and Research
  • 24. Institut de Myologie
  • 25. Sorbonne Université
  • 26. Celescreen (France)
  • 27. Hôpital de la Timone

Description

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

⚠️ This is an automatic machine translation with an accuracy of 90-95%

Translated Description (Arabic)

تم نشر تعديل على هذه الورقة ويمكن الوصول إليه عبر رابط في أعلى الورقة.

Translated Description (French)

Un amendement à ce document a été publié et est accessible via un lien en haut du document.

Translated Description (Spanish)

Se ha publicado una enmienda a este documento y se puede acceder a ella a través de un enlace en la parte superior del documento.

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Additional details

Additional titles

Translated title (Arabic)
تصحيح المؤلف: فقدان MTX2 يسبب خلل تنسج الفك السفلي العجزي ويربط خلل الميتوكوندريا بالتشكل النووي المتغير
Translated title (French)
Correction de l'auteur : La perte de MTX2 provoque une dysplasie mandibuloacrée et relie le dysfonctionnement mitochondrial à une morphologie nucléaire altérée
Translated title (Spanish)
Corrección del autor: La pérdida de MTX2 causa displasia mandibuloacral y vincula la disfunción mitocondrial con una morfología nuclear alterada

Identifiers

Other
https://openalex.org/W3093077820
DOI
10.1038/s41467-020-19290-y

Is supplement to
https://openalex.org/W4234157524 (Other)
https://openalex.org/W2788277189 (Other)
https://openalex.org/W2151865869 (Other)
https://openalex.org/W2130076355 (Other)
https://openalex.org/W2119695867 (Other)
https://openalex.org/W2117258802 (Other)
https://openalex.org/W2082860237 (Other)
https://openalex.org/W2013243191 (Other)
https://openalex.org/W1993764875 (Other)
https://openalex.org/W1990804418 (Other)

GreSIS Basics Section

Is Global South Knowledge
Yes
Country
Egypt