Molecular Mechanisms of Synaptic Dysregulation in Fragile X Syndrome and Autism Spectrum Disorders

Fragile X syndrome (FXS) is the most common form of monogenic hereditary cognitive impairment. FXS patient exhibit a high comorbidity rate with autism spectrum disorders (ASDs). This makes FXS a model disease for understanding how synaptic dysregulation alters neuronal excitability, learning and mem...

Descripción completa

Detalles Bibliográficos
Autor principal: Telias, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417395/
https://www.ncbi.nlm.nih.gov/pubmed/30899214
http://dx.doi.org/10.3389/fnmol.2019.00051

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417395/
https://www.ncbi.nlm.nih.gov/pubmed/30899214
http://dx.doi.org/10.3389/fnmol.2019.00051

Ejemplares similares