Mutations in SMARCB1 and in other Coffin–Siris syndrome genes lead to various brain midline defects

Mutations in genes encoding components of BAF (BRG1/BRM-associated factor) chromatin remodeling complexes cause neurodevelopmental disorders and tumors. The mechanisms leading to the development of these two disease entities alone or in combination remain unclear. We generated mice with a heterozygo...

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Detalles Bibliográficos
Autores principales: Filatova, Alina, Rey, Linda K., Lechler, Marion B., Schaper, Jörg, Hempel, Maja, Posmyk, Renata, Szczaluba, Krzysztof, Santen, Gijs W. E., Wieczorek, Dagmar, Nuber, Ulrike A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609698/
https://www.ncbi.nlm.nih.gov/pubmed/31273213
http://dx.doi.org/10.1038/s41467-019-10849-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609698/
https://www.ncbi.nlm.nih.gov/pubmed/31273213
http://dx.doi.org/10.1038/s41467-019-10849-y

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