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Oxytocin improves behavioral and electrophysiological deficits in a novel Shank3-deficient rat
Mutations in the synaptic gene SHANK3 lead to a neurodevelopmental disorder known as Phelan-McDermid syndrome (PMS). PMS is a relatively common monogenic and highly penetrant cause of autism spectrum disorder (ASD) and intellectual disability (ID), and frequently presents with attention deficits. Th...
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| Publicado no: | eLife |
|---|---|
| Main Authors: | , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
eLife Sciences Publications, Ltd
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5283828/ https://ncbi.nlm.nih.gov/pubmed/28139198 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.18904 |
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