SYNGAP1 Controls the Maturation of Dendrites, Synaptic Function, and Network Activity in Developing Human Neurons

SYNGAP1 is a major genetic risk factor for global developmental delay, autism spectrum disorder, and epileptic encephalopathy. De novo loss-of-function variants in this gene cause a neurodevelopmental disorder defined by cognitive impairment, social-communication disorder, and early-onset seizures....

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:J Neurosci
Asıl Yazarlar: Llamosas, Nerea, Arora, Vineet, Vij, Ridhima, Kilinc, Murat, Bijoch, Lukasz, Rojas, Camilo, Reich, Adrian, Sridharan, BanuPriya, Willems, Erik, Piper, David R., Scampavia, Louis, Spicer, Timothy P., Miller, Courtney A., Holder, J. Lloyd, Rumbaugh, Gavin
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Society for Neuroscience 2020
Konular:
Research Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7548701/
https://ncbi.nlm.nih.gov/pubmed/32887745
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.1367-20.2020
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller