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Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.
Elouej, Sahar; Harhouri, Karim; Mao, Morgane Le; Baujat, Genevieve; Nampoothiri, Sheela; Kayserili, Hϋlya; Menabawy, Nihal Al; Selim, Laila; Paneque, Arianne Llamos; Kubisch, Christian; Lessel, Davor; Rubinsztajn, Robert; Charar, Chayki; Bartoli, Catherine; Airault, Coraline; Deleuze, Jean-François; Rötig, Agnes; Bauer, Peter; Pereira, Catarina; Loh, Abigail; Escande-Beillard, Nathalie; Muchir, Antoine; Martino, Lisa; Gruenbaum, Yosef; Lee, Song-Hua; Manivet, Philippe; Lenaers, Guy; Reversade, Bruno; Lévy, Nicolas; De Sandre-Giovannoli, Annachiara.
Afiliação
  • Elouej S; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.
  • Harhouri K; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.
  • Mao ML; MitoLab, Mitochondrial Medicine Research Centre, Institut MITOVASC, CNRS UMR 6015, INSERM U1083, Université d'Angers, CHU d'Angers, Angers, France.
  • Baujat G; Department of Medical Genetics, INSERM UMR 1163, Paris Descartes-Sorbonne Paris Cité University, IMAGINE Institute, Necker Enfants Malades Hospital, Paris, France.
  • Nampoothiri S; Department of Pediatric Genetics, Amrita Institute of Medical Sciences & Research Centre, AIMS Ponekkara PO Cochin, Kerala, India.
  • Kayserili H; Medical Genetics Department, Koç University, School of Medicine (KUSoM), Istanbul, Turkey.
  • Menabawy NA; Neurology and Metabolic Division, Cairo University Children Hospital, Cairo, Egypt.
  • Selim L; Neurology and Metabolic Division, Cairo University Children Hospital, Cairo, Egypt.
  • Paneque AL; Medical Genetics Service Specialties Hospital FF AA No.1, Quito, Ecuador.
  • Kubisch C; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Lessel D; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Rubinsztajn R; Pole of Anesthesiology and Reanimation, , Necker Enfants Malades Hospital, Paris, France.
  • Charar C; Department of Genetics, Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
  • Bartoli C; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.
  • Airault C; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.
  • Deleuze JF; 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.
  • Rötig A; INSERM UMR1163, Institut Imagine, Paris, France.
  • Bauer P; CENTOGENE AG, Rostock, Germany.
  • Pereira C; CENTOGENE AG, Rostock, Germany.
  • Loh A; Institute of Medical Biology, A*STAR, Singapore, Singapore.
  • Escande-Beillard N; Medical Genetics Department, Koç University, School of Medicine (KUSoM), Istanbul, Turkey.
  • Muchir A; Institute of Medical Biology, A*STAR, Singapore, Singapore.
  • Martino L; Sorbonne Université, INSERM, Institute of Myology, Center of Research in Myology, Paris, France.
  • Gruenbaum Y; CeleScreen SAS, Paris, France.
  • Lee SH; Department of Genetics, Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
  • Manivet P; CeleScreen SAS, Paris, France.
  • Lenaers G; CeleScreen SAS, Paris, France.
  • Reversade B; APHP, Biobank Lariboisière BB-0033-00064, Platform of BioPathology and Innovative Technologies in Health, Hôpital Lariboisière, Paris, France.
  • Lévy N; INSERM UMR1141 « NeuroDiderot ¼, Université de Paris, Paris, France.
  • De Sandre-Giovannoli A; MitoLab, Mitochondrial Medicine Research Centre, Institut MITOVASC, CNRS UMR 6015, INSERM U1083, Université d'Angers, CHU d'Angers, Angers, France.
Nat Commun ; 11(1): 5349, 2020 Oct 19.
Article em En | MEDLINE | ID: mdl-33077719
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: França
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: França