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Author correction: loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology

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dc.contributor.coauthorElouej, Sahar
dc.contributor.coauthorHarhouri, Karim
dc.contributor.coauthorMao, Morgane Le
dc.contributor.coauthorBaujat, Genevieve
dc.contributor.coauthorNampoothiri, Sheela
dc.contributor.coauthorMenabawy, Nihal Al
dc.contributor.coauthorSelim, Laila
dc.contributor.coauthorPaneque, Arianne Llamos
dc.contributor.coauthorKubisch, Christian
dc.contributor.coauthorLessel, Davor
dc.contributor.coauthorRubinsztajn, Robert
dc.contributor.coauthorCharar, Chayki
dc.contributor.coauthorBartoli, Catherine
dc.contributor.coauthorAirault, Coraline
dc.contributor.coauthorDeleuze, Jean-François
dc.contributor.coauthorRötig, Agnes
dc.contributor.coauthorBauer, Peter
dc.contributor.coauthorPereira, Catarina
dc.contributor.coauthorLoh, Abigail
dc.contributor.coauthorMuchir, Antoine
dc.contributor.coauthorMartino, Lisa
dc.contributor.coauthorGruenbaum, Yosef
dc.contributor.coauthorLee, Song-Hua
dc.contributor.coauthorManivet, Philippe
dc.contributor.coauthorLenaers, Guy
dc.contributor.coauthorLévy, Nicolas
dc.contributor.coauthorDe Sandre-Giovannoli, Annachiara
dc.contributor.departmentSchool of Medicine
dc.contributor.facultymemberYes
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.kuauthorBeillard, Nathalie Sonia Escande
dc.contributor.kuauthorReversade, Bruno
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:36:53Z
dc.date.issued2020
dc.description.abstractThe original version of this Article contained errors in the author affiliations. The affiliations of Nathalie Escande-Beillard and Bruno Reversade with ‘Medical Genetics Department, Koç University, School of Medicine (KUSoM), Istanbul, Turkey’ were inadvertently omitted. This has now been corrected in both the PDF and HTML versions of the Article.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessYES
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.doi10.1038/s41467-020-19290-y
dc.identifier.eissn2041-1723
dc.identifier.embargoN/A
dc.identifier.issn2041-1723
dc.identifier.issue1
dc.identifier.pubmed33077719
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85092796538
dc.identifier.urihttps://doi.org/10.1038/s41467-020-19290-y
dc.identifier.urihttps://hdl.handle.net/20.500.14288/12735
dc.identifier.volume11
dc.identifier.wos000585920300001
dc.keywordsMTX2
dc.keywordsMetaxin 2
dc.keywordsMandibuloacral dysplasia
dc.keywordsMitochondrial dysfunction
dc.keywordsNuclear morphology
dc.keywordsProgeroid syndrome
dc.keywordsGenetic disorders
dc.keywordsPremature aging
dc.keywordsMitochondria
dc.keywordsNuclear envelope
dc.keywordsRare disease
dc.keywordsAuthor correction
dc.language.isoeng
dc.publisherNature Portfolio
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofNature Communications
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectGenetics
dc.subjectCell biology
dc.subjectMedical genetics
dc.subjectMolecular biology
dc.titleAuthor correction: loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology
dc.typeOther
dspace.entity.typePublication
local.contributor.kuauthorKayserili, Hülya
local.contributor.kuauthorBeillard, Nathalie Sonia Escande
local.contributor.kuauthorReversade, Bruno
relation.isOrgUnitOfPublicationd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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