Publication:
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.coauthorLe Mao, Morgane
dc.contributor.coauthorBaujat, Genevieve
dc.contributor.coauthorNampoothiri, Sheela
dc.contributor.coauthoral Menabawy, Nihal
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-Francois
dc.contributor.coauthorRotig, 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.coauthorLevy, Nicolas
dc.contributor.coauthorDe Sandre-Giovannoli, Annachiara
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.kuauthorBeillard, Nathalie Sonia Escande
dc.contributor.kuauthorReversade, Bruno
dc.contributor.kuprofileFaculty Member
dc.contributor.kuprofileResearcher
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.yokid7945
dc.contributor.yokidN/A
dc.contributor.yokid274182
dc.date.accessioned2024-11-09T23:36:53Z
dc.date.issued2020
dc.description.abstractN/A
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue1
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.volume11
dc.identifier.doi10.1038/s41467-020-19290-y
dc.identifier.issn2041-1723
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85092796538
dc.identifier.urihttp://dx.doi.org/10.1038/s41467-020-19290-y
dc.identifier.urihttps://hdl.handle.net/20.500.14288/12735
dc.identifier.wos585920300001
dc.languageEnglish
dc.publisherNature Research
dc.sourceNature Communications
dc.subjectMultidisciplinary sciences
dc.titleLoss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology
dc.typeOther
dc.type.otherCorrection
dspace.entity.typePublication
local.contributor.authorid0000-0003-0376-499X
local.contributor.authorid0000-0002-7706-1608
local.contributor.authorid0000-0002-4070-7997
local.contributor.kuauthorKayserili, Hülya
local.contributor.kuauthorBeillard, Nathalie Sonia Escande
local.contributor.kuauthorReversade, Bruno

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