Publication: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology
| dc.contributor.coauthor | Elouej, Sahar | |
| dc.contributor.coauthor | Harhouri, Karim | |
| dc.contributor.coauthor | Le Mao, Morgane | |
| dc.contributor.coauthor | Baujat, Genevieve | |
| dc.contributor.coauthor | Nampoothiri, Sheela | |
| dc.contributor.coauthor | al Menabawy, Nihal | |
| dc.contributor.coauthor | Selim, Laila | |
| dc.contributor.coauthor | Paneque, Arianne Llamos | |
| dc.contributor.coauthor | Kubisch, Christian | |
| dc.contributor.coauthor | Lessel, Davor | |
| dc.contributor.coauthor | Rubinsztajn, Robert | |
| dc.contributor.coauthor | Charar, Chayki | |
| dc.contributor.coauthor | Bartoli, Catherine | |
| dc.contributor.coauthor | airault, Coraline | |
| dc.contributor.coauthor | Deleuze, Jean-Francois | |
| dc.contributor.coauthor | Rotig, Agnes | |
| dc.contributor.coauthor | Bauer, Peter | |
| dc.contributor.coauthor | Pereira, Catarina | |
| dc.contributor.coauthor | Loh, Abigail | |
| dc.contributor.coauthor | Muchir, Antoine | |
| dc.contributor.coauthor | Martino, Lisa | |
| dc.contributor.coauthor | Gruenbaum, Yosef | |
| dc.contributor.coauthor | Lee, Song-Hua | |
| dc.contributor.coauthor | Manivet, Philippe | |
| dc.contributor.coauthor | Lenaers, Guy | |
| dc.contributor.coauthor | Levy, Nicolas | |
| dc.contributor.coauthor | De Sandre-Giovannoli, Annachiara | |
| dc.contributor.department | School of Medicine | |
| dc.contributor.kuauthor | Beillard, Nathalie Sonia Escande | |
| dc.contributor.kuauthor | Kayserili, Hülya | |
| dc.contributor.kuauthor | Reversade, Bruno | |
| dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
| dc.date.accessioned | 2024-11-09T23:36:53Z | |
| dc.date.issued | 2020 | |
| dc.description.indexedby | WOS | |
| dc.description.indexedby | Scopus | |
| dc.description.indexedby | PubMed | |
| dc.description.issue | 1 | |
| dc.description.openaccess | YES | |
| dc.description.publisherscope | International | |
| dc.description.sponsoredbyTubitakEu | N/A | |
| dc.description.volume | 11 | |
| dc.identifier.doi | 10.1038/s41467-020-19290-y | |
| dc.identifier.issn | 2041-1723 | |
| dc.identifier.quartile | Q1 | |
| dc.identifier.scopus | 2-s2.0-85092796538 | |
| dc.identifier.uri | https://doi.org/10.1038/s41467-020-19290-y | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14288/12735 | |
| dc.identifier.wos | 585920300001 | |
| dc.language.iso | eng | |
| dc.publisher | Nature Research | |
| dc.relation.ispartof | Nature Communications | |
| dc.subject | Multidisciplinary sciences | |
| dc.title | Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology | |
| dc.type | Other | |
| dc.type.other | Correction | |
| dspace.entity.type | Publication | |
| local.contributor.kuauthor | Kayserili, Hülya | |
| local.contributor.kuauthor | Beillard, Nathalie Sonia Escande | |
| local.contributor.kuauthor | Reversade, Bruno | |
| local.publication.orgunit1 | SCHOOL OF MEDICINE | |
| local.publication.orgunit2 | School of Medicine | |
| person.familyName | Beillard | |
| person.familyName | Kayserili | |
| person.familyName | Reversade | |
| person.givenName | Nathalie Sonia Escande | |
| person.givenName | Hülya | |
| person.givenName | Bruno | |
| relation.isOrgUnitOfPublication | d02929e1-2a70-44f0-ae17-7819f587bedd | |
| relation.isOrgUnitOfPublication.latestForDiscovery | d02929e1-2a70-44f0-ae17-7819f587bedd | |
| relation.isParentOrgUnitOfPublication | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e | |
| relation.isParentOrgUnitOfPublication.latestForDiscovery | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e |
