CC2D1A Regulates Human Intellectual and Social Function as well as NF-κB Signaling Homeostasis

Autism spectrum disorder (ASD) and intellectual disability (ID) are often comorbid, but the extent to which they share common genetic causes remains controversial. Here, we present two autosomal-recessive “founder” mutations in the CC2D1A gene causing fully penetrant cognitive phenotypes, including...

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Detalles Bibliográficos
Autores principales: Manzini, M. Chiara, Xiong, Lan, Shaheen, Ranad, Tambunan, Dimira E., Di Costanzo, Stefania, Mitisalis, Vanessa, Tischfield, David J., Cinquino, Antonella, Ghaziuddin, Mohammed, Christian, Mehtab, Jiang, Qin, Laurent, Sandra, Nanjiani, Zohair A., Rasheed, Saima, Hill, R. Sean, Lizarraga, Sofia B., Gleason, Danielle, Sabbagh, Diya, Salih, Mustafa A., Alkuraya, Fowzan S., Walsh, Christopher A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334362/
https://www.ncbi.nlm.nih.gov/pubmed/25066123
http://dx.doi.org/10.1016/j.celrep.2014.06.039

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334362/
https://www.ncbi.nlm.nih.gov/pubmed/25066123
http://dx.doi.org/10.1016/j.celrep.2014.06.039

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