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.license | open | en_US |
| dc.contributor.author | DE BOER, Elke | |
| dc.contributor.author | OCKELOEN, Charlotte W. | |
| dc.contributor.author | MATALONGA, Leslie | |
| dc.contributor.author | HORVATH, Rita | |
| dc.contributor.author | SOLVE-RD SNV-INDEL, Working Group | |
| dc.contributor.author | RODENBURG, Richard J. | |
| dc.contributor.author | COENEN, Marieke J. H. | |
| dc.contributor.author | JANSSEN, Mirian | |
| dc.contributor.author | HENSSEN, Dylan | |
| dc.contributor.author | GILISSEN, Christian | |
| dc.contributor.author | STEYAERT, Wouter | |
| dc.contributor.author | PARAMONOV, Ida | |
| dc.contributor.author | SOLVE-RD, DITF-ITHACA | |
| hal.structure.identifier | Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM] | |
| dc.contributor.author | TRIMOUILLE, Aurelien | |
| dc.contributor.author | KLEEFSTRA, Tjitske | |
| dc.contributor.author | VERLOES, Alain | |
| dc.contributor.author | VISSERS, Lisenka E. L. M. | |
| dc.date.accessioned | 2021-10-26T09:21:10Z | |
| dc.date.available | 2021-10-26T09:21:10Z | |
| dc.date.issued | 2021-07-15 | |
| dc.identifier.issn | 1476-5438 (online) 1018-4813 (print) | en_US |
| dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/112877 | |
| dc.description.abstractEn | In the original publication of the article, consortium author lists were missing in the article. The details are as below. | |
| dc.language.iso | EN | en_US |
| dc.title.en | 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.type | Article de revue | en_US |
| dc.identifier.doi | 10.1038/s41431-021-00937-3 | en_US |
| dc.subject.hal | Sciences du Vivant [q-bio]/Médecine humaine et pathologie | en_US |
| dc.identifier.pubmed | 34267341 | en_US |
| bordeaux.journal | European Journal of Human Genetics | en_US |
| bordeaux.page | 1470-1471 | en_US |
| bordeaux.volume | 29 | en_US |
| bordeaux.hal.laboratories | Maladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211 | en_US |
| bordeaux.issue | 9 | en_US |
| bordeaux.institution | Université de Bordeaux | en_US |
| bordeaux.institution | INSERM | en_US |
| bordeaux.peerReviewed | oui | en_US |
| bordeaux.inpress | non | en_US |
| hal.identifier | hal-03403537 | |
| hal.version | 1 | |
| hal.date.transferred | 2021-10-26T09:21:16Z | |
| hal.export | true | |
| dc.rights.cc | Pas de Licence CC | en_US |
| bordeaux.COinS | ctx_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 |
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