DYT1 dystonia increases risk taking in humans

It has been difficult to link synaptic modification to overt behavioral changes. Rodent models of DYT1 dystonia, a motor disorder caused by a single gene mutation, demonstrate increased long-term potentiation and decreased long-term depression in corticostriatal synapses. Computationally, such asymm...

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Detalles Bibliográficos
Autores principales: Arkadir, David, Radulescu, Angela, Raymond, Deborah, Lubarr, Naomi, Bressman, Susan B, Mazzoni, Pietro, Niv, Yael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951192/
https://www.ncbi.nlm.nih.gov/pubmed/27249418
http://dx.doi.org/10.7554/eLife.14155

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951192/
https://www.ncbi.nlm.nih.gov/pubmed/27249418
http://dx.doi.org/10.7554/eLife.14155

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