Chromatin remodeller CHD7 is required for GABAergic neuron development by promoting PAQR3 expression

Mutations in the chromatin remodeller‐coding gene CHD7 cause CHARGE syndrome (CS). CS features include moderate to severe neurological and behavioural problems, clinically characterized by intellectual disability, attention‐deficit/hyperactivity disorder and autism spectrum disorder. To investigate...

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Detalles Bibliográficos
Autores principales: Jamadagni, Priyanka, Breuer, Maximilian, Schmeisser, Kathrin, Cardinal, Tatiana, Kassa, Betelhem, Parker, J Alex, Pilon, Nicolas, Samarut, Eric, Patten, Shunmoogum A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183419/
https://www.ncbi.nlm.nih.gov/pubmed/33900016
http://dx.doi.org/10.15252/embr.202050958

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183419/
https://www.ncbi.nlm.nih.gov/pubmed/33900016
http://dx.doi.org/10.15252/embr.202050958

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