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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Publicat a:Hum Mol Genet
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2017
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Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5437529/
https://ncbi.nlm.nih.gov/pubmed/28334947
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddx094
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