Mouse Cntnap2 and Human CNTNAP2 ASD Alleles Cell Autonomously Regulate PV(+) Cortical Interneurons

Human mutations in CNTNAP2 are associated with an array of neuropsychiatric and neurological syndromes, including speech and language disorders, epilepsy, and autism spectrum disorder (ASD). We examined Cntnap2’s expression and function in GABAergic cortical interneurons (CINs), where its RNA is pre...

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Detalhes bibliográficos
Publicado no:Cereb Cortex
Main Authors: Vogt, Daniel, Cho, Kathleen K A, Shelton, Samantha M, Paul, Anirban, Huang, Z Josh, Sohal, Vikaas S, Rubenstein, John L R
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6455910/
https://ncbi.nlm.nih.gov/pubmed/29028946
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cercor/bhx248
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