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Author Correction: CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder.

dc.rights.licenseopenen_US
dc.contributor.authorDE THONEL, Aurélie
dc.contributor.authorAHLSKOG, Johanna K
dc.contributor.authorDAUPIN, Kevin
dc.contributor.authorDUBREUIL, Véronique
dc.contributor.authorBERTHELET, Jérémy
dc.contributor.authorCHAPUT, Carole
dc.contributor.authorPIRES, Geoffrey
dc.contributor.authorLEONETTI, Camille
dc.contributor.authorABANE, Ryma
dc.contributor.authorBARRIS, Lluís Cordón
dc.contributor.authorLERAY, Isabelle
dc.contributor.authorAALTO, Anna L
dc.contributor.authorNACERI, Sarah
dc.contributor.authorCORDONNIER, Marine
dc.contributor.authorBENASOLO, Carène
dc.contributor.authorSANIAL, Matthieu
dc.contributor.authorDUCHATEAU, Agathe
dc.contributor.authorVIHERVAARA, Anniina
dc.contributor.authorPUUSTINEN, Mikael C
dc.contributor.authorMIOZZO, Federico
hal.structure.identifierLaboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
dc.contributor.authorFERGELOT, Patricia
dc.contributor.authorLEBIGOT, Élise
dc.contributor.authorVERLOES, Alain
dc.contributor.authorGRESSENS, Pierre
hal.structure.identifierLaboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
dc.contributor.authorLACOMBE, Didier
dc.contributor.authorGOBBO, Jessica
dc.contributor.authorGARRIDO, Carmen
dc.contributor.authorWESTERHEIDE, Sandy D
dc.contributor.authorDAVID, Laurent
dc.contributor.authorPETITJEAN, Michel
dc.contributor.authorTABOUREAU, Olivier
dc.contributor.authorRODRIGUES-LIMA, Fernando
dc.contributor.authorPASSEMARD, Sandrine
dc.contributor.authorSABÉRAN-DJONEIDI, Délara
dc.contributor.authorNGUYEN, Laurent
dc.contributor.authorLANCASTER, Madeline
dc.contributor.authorSISTONEN, Lea
dc.contributor.authorMEZGER, Valérie
dc.date.accessioned2024-02-15T16:40:08Z
dc.date.available2024-02-15T16:40:08Z
dc.date.issued2023-09-28
dc.identifier.issn2041-1723en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/188171
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.title.enAuthor Correction: CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder.
dc.title.alternativeNat Communen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1038/s41467-023-41869-4en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed37770591en_US
bordeaux.journalNature Communicationsen_US
bordeaux.page6067en_US
bordeaux.volume14en_US
bordeaux.hal.laboratoriesMaladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04460445
hal.version1
hal.date.transferred2024-02-15T16:40:38Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccCC BYen_US
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