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Striatopallidal dysfunction underlies repetitive behavior in Shank3-deficient model of autism
The postsynaptic scaffolding protein SH3 and multiple ankyrin repeat domains 3 (SHANK3) is critical for the development and function of glutamatergic synapses. Disruption of the SHANK3-encoding gene has been strongly implicated as a monogenic cause of autism, and Shank3 mutant mice show repetitive g...
Guardat en:
| Publicat a: | J Clin Invest |
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| Autors principals: | , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5409790/ https://ncbi.nlm.nih.gov/pubmed/28414301 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI87997 |
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