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....

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Publicat a:J Neurosci
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Society for Neuroscience 2020
Matèries:
Research Articles
Accés en línia: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
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