- Title
- Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology
- Creators - without role
- Sahar Elouej - Aix-Marseille UniversityKarim Harhouri - Aix-Marseille UniversityMorgane Le Mao - InsermGenevieve Baujat - Délégation Paris 5Sheela Nampoothiri - Amrita Institute of Medical Sciences and Research CentreHϋlya Kayserili - Istanbul, TurkeyNihal Al Menabawy - Cairo, EgyptLaila Selim - Cairo UniversityArianne Llamos Paneque - Medical Genetics CenterChristian Kubisch - University Medical Center Hamburg-EppendorfDavor Lessel - University Medical Center Hamburg-EppendorfRobert Rubinsztajn - Paris, FranceChayki Charar - Hebrew University of JerusalemCatherine Bartoli - Aix-Marseille UniversityCoraline Airault - Aix-Marseille UniversityJean-François Deleuze - Fondation Jean Dausset-CEPHAgnes Rötig - Imagine Institute for Genetic DiseasesPeter Bauer - CentogeneCatarina Pereira - CentogeneAbigail Loh - Institute of Medical BiologyNathalie Escande-Beillard - Institute of Medical BiologyAntoine Muchir - Institut de MyologieLisa Martino - CelescreenYosef Gruenbaum - Hebrew University of JerusalemSong-Hua Lee - CelescreenPhilippe Manivet - Délégation Paris 7Guy Lenaers - Université d'AngersBruno Reversade - Institute of Medical BiologyNicolas Lévy - Aix-Marseille UniversityAnnachiara De Sandre-Giovannoli - Aix-Marseille University
- Publication Details
- Nature communications, Vol.11(1), pp.5349-5349
- Publisher
- Nature Publishing Group UK
- Identifiers
- 9944956808331
- Academic Unit
- King Abdullah University of Science & Technology
- Language
- English
- Resource Type
- Journal article
Journal article
Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology
Nature communications, Vol.11(1), pp.5349-5349
19/10/2020
PMCID: 7572408
PMID: 33077719
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