Afficher la notice abrégée

Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

dc.rights.licenseopenen_US
dc.contributor.authorDE BOER, Elke
dc.contributor.authorOCKELOEN, Charlotte W.
dc.contributor.authorMATALONGA, Leslie
dc.contributor.authorHORVATH, Rita
dc.contributor.authorSOLVE-RD SNV-INDEL, Working Group
dc.contributor.authorRODENBURG, Richard J.
dc.contributor.authorCOENEN, Marieke J. H.
dc.contributor.authorJANSSEN, Mirian
dc.contributor.authorHENSSEN, Dylan
dc.contributor.authorGILISSEN, Christian
dc.contributor.authorSTEYAERT, Wouter
dc.contributor.authorPARAMONOV, Ida
dc.contributor.authorSOLVE-RD, DITF-ITHACA
hal.structure.identifierLaboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
dc.contributor.authorTRIMOUILLE, Aurelien
dc.contributor.authorKLEEFSTRA, Tjitske
dc.contributor.authorVERLOES, Alain
dc.contributor.authorVISSERS, Lisenka E. L. M.
dc.date.accessioned2021-10-26T09:21:10Z
dc.date.available2021-10-26T09:21:10Z
dc.date.issued2021-07-15
dc.identifier.issn1476-5438 (online) 1018-4813 (print)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/112877
dc.description.abstractEnIn the original publication of the article, consortium author lists were missing in the article. The details are as below.
dc.language.isoENen_US
dc.title.enCorrection: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)
dc.typeArticle de revueen_US
dc.identifier.doi10.1038/s41431-021-00937-3en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed34267341en_US
bordeaux.journalEuropean Journal of Human Geneticsen_US
bordeaux.page1470-1471en_US
bordeaux.volume29en_US
bordeaux.hal.laboratoriesMaladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211en_US
bordeaux.issue9en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03403537
hal.version1
hal.date.transferred2021-10-26T09:21:16Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=European%20Journal%20of%20Human%20Genetics&rft.date=2021-07-15&rft.volume=29&rft.issue=9&rft.spage=1470-1471&rft.epage=1470-1471&rft.eissn=1476-5438%20(online)%201018-4813%20(print)&rft.issn=1476-5438%20(online)%201018-4813%20(print)&rft.au=DE%20BOER,%20Elke&OCKELOEN,%20Charlotte%20W.&MATALONGA,%20Leslie&HORVATH,%20Rita&SOLVE-RD%20SNV-INDEL,%20Working%20Group&rft.genre=article


Fichier(s) constituant ce document

FichiersTailleFormatVue

Il n'y a pas de fichiers associés à ce document.

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée