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Hypersociability in the Angelman syndrome mouse model
Deletions and reciprocal triplications of the human chromosomal 15q11-13 region cause two distinct neurodevelopmental disorders. Maternally-derived deletions or inactivating mutations of UBE3A, a 15q11-13 gene expressed exclusively from the maternal allele in neurons, cause Angelman syndrome, charac...
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| Publicado no: | Exp Neurol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5484625/ https://ncbi.nlm.nih.gov/pubmed/28411125 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.expneurol.2017.04.002 |
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