CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2041-1723
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder ; volume:13 ; number:1 ; day:16 ; month:11 ; year:2022 ; pages:1-21 ; date:12.2022
Nature Communications ; 13, Heft 1 (16.11.2022), 1-21, 12.2022
- Creator
-
Thonel, Aurélie de
Ahlskog, Johanna K.
Daupin, Kevin
Dubreuil, Véronique
Berthelet, Jérémy
Chaput, Carole
Pires, Geoffrey
Leonetti, Camille
Abane, Ryma
Barris, Lluís Cordón
Leray, Isabelle
Aalto, Anna L.
Naceri, Sarah
Cordonnier, Marine
Benasolo, Carène
Sanial, Matthieu
Duchateau, Agathe
Vihervaara, Anniina
Puustinen, Mikael C.
Miozzo, Federico
Fergelot, Patricia
Lebigot, Élise
Verloes, Alain
Gressens, Pierre
Lacombe, Didier
Gobbo, Jessica
Garrido, Carmen
Westerheide, Sandy D.
David, Laurent
Petitjean, Michel
Taboureau, Olivier
Rodrigues-Lima, Fernando
Passemard, Sandrine
Sabéran-Djoneidi, Délara
Nguyen, Laurent
Lancaster, Madeline
Sistonen, Lea
Mezger, Valérie
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-022-34476-2
- URN
-
urn:nbn:de:101:1-2023012909153545297326
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:24 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Thonel, Aurélie de
- Ahlskog, Johanna K.
- Daupin, Kevin
- Dubreuil, Véronique
- Berthelet, Jérémy
- Chaput, Carole
- Pires, Geoffrey
- Leonetti, Camille
- Abane, Ryma
- Barris, Lluís Cordón
- Leray, Isabelle
- Aalto, Anna L.
- Naceri, Sarah
- Cordonnier, Marine
- Benasolo, Carène
- Sanial, Matthieu
- Duchateau, Agathe
- Vihervaara, Anniina
- Puustinen, Mikael C.
- Miozzo, Federico
- Fergelot, Patricia
- Lebigot, Élise
- Verloes, Alain
- Gressens, Pierre
- Lacombe, Didier
- Gobbo, Jessica
- Garrido, Carmen
- Westerheide, Sandy D.
- David, Laurent
- Petitjean, Michel
- Taboureau, Olivier
- Rodrigues-Lima, Fernando
- Passemard, Sandrine
- Sabéran-Djoneidi, Délara
- Nguyen, Laurent
- Lancaster, Madeline
- Sistonen, Lea
- Mezger, Valérie
- SpringerLink (Online service)
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Author Correction: CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
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Further delineation of the SCAF4-associated neurodevelopmental disorder
PACS1-Neurodevelopmental disorder: clinical features and trial readiness
Best Practices in Structural Neuroimaging of Neurodevelopmental Disorders
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder
Investigating the impact of the environment on neurodevelopmental disorder
STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
Neurodevelopmental profile of Fetal Alcohol Spectrum Disorder: A systematic review
Complex interplay of neurodevelopmental disorders (NDDs), fractures, and osteoporosis: a mendelian randomization study
Author Correction: CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Neurodevelopmental disorder associated with the DOCK7 gene
Functional characterization of TBR1 variants in neurodevelopmental disorder
Further delineation of the SCAF4-associated neurodevelopmental disorder
PACS1-Neurodevelopmental disorder: clinical features and trial readiness
Best Practices in Structural Neuroimaging of Neurodevelopmental Disorders
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder
Investigating the impact of the environment on neurodevelopmental disorder
STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
Neurodevelopmental profile of Fetal Alcohol Spectrum Disorder: A systematic review