Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERα)

De novo and inherited mutations of X-chromosome cell adhesion molecule protocadherin 19 (PCDH19) cause frequent, highly variable epilepsy, autism, cognitive decline and behavioural problems syndrome. Intriguingly, hemizygous null males are not affected while heterozygous females are, contradicting e...

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Detalles Bibliográficos
Autores principales: Pham, Duyen H., Tan, Chuan C., Homan, Claire C., Kolc, Kristy L., Corbett, Mark A., McAninch, Dale, Fox, Archa H., Thomas, Paul Q., Kumar, Raman, Gecz, Jozef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437529/
https://www.ncbi.nlm.nih.gov/pubmed/28334947
http://dx.doi.org/10.1093/hmg/ddx094

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437529/
https://www.ncbi.nlm.nih.gov/pubmed/28334947
http://dx.doi.org/10.1093/hmg/ddx094

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