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Author Correction: CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder.
Nat Commun. 2023 Sep 28;14(1):6067. doi: 10.1038/s41467-023-41869-4.
Nat Commun. 2023.
PMID: 37770591
Free PMC article.
No abstract available.
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder.
de Thonel A, Ahlskog JK, Daupin K, Dubreuil V, Berthelet J, Chaput C, Pires G, Leonetti C, Abane R, Barris LC, Leray I, Aalto AL, Naceri S, Cordonnier M, Benasolo C, Sanial M, Duchateau A, Vihervaara A, Puustinen MC, Miozzo F, Fergelot P, Lebigot É, Verloes A, Gressens P, Lacombe D, Gobbo J, Garrido C, Westerheide SD, David L, Petitjean M, Taboureau O, Rodrigues-Lima F, Passemard S, Sabéran-Djoneidi D, Nguyen L, Lancaster M, Sistonen L, Mezger V.
de Thonel A, et al. Among authors: daupin k.
Nat Commun. 2022 Nov 16;13(1):7002. doi: 10.1038/s41467-022-34476-2.
Nat Commun. 2022.
PMID: 36385105
Free PMC article.
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Loss of function mutation of Eftud2, the gene responsible for mandibulofacial dysostosis with microcephaly (MFDM), leads to pre-implantation arrest in mouse.
Beauchamp MC, Djedid A, Daupin K, Clokie K, Kumar S, Majewski J, Jerome-Majewska LA.
Beauchamp MC, et al. Among authors: daupin k.
PLoS One. 2019 Jul 5;14(7):e0219280. doi: 10.1371/journal.pone.0219280. eCollection 2019.
PLoS One. 2019.
PMID: 31276534
Free PMC article.
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