Synaptic Alterations in a Transgenic Model of Tuberous Sclerosis Complex: Relevance to Autism Spectrum Disorders

Tuberous sclerosis complex (TSC) is a rare, multi-system genetic disease with serious neurological and mental symptoms, including autism. Mutations in the TSC1/TSC2 genes lead to the overactivation of mTOR signalling, which is also linked to nonsyndromic autism. Our aim was to analyse synaptic patho...

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Detalles Bibliográficos
Autores principales: Czapski, Grzegorz A., Babiec, Lidia, Jęśko, Henryk, Gąssowska-Dobrowolska, Magdalena, Cieślik, Magdalena, Matuszewska, Marta, Frontczak-Baniewicz, Małgorzata, Zajdel, Karolina, Adamczyk, Agata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466868/
https://www.ncbi.nlm.nih.gov/pubmed/34576223
http://dx.doi.org/10.3390/ijms221810058

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466868/
https://www.ncbi.nlm.nih.gov/pubmed/34576223
http://dx.doi.org/10.3390/ijms221810058

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