A carregar...
Enhanced Transmission at the Calyx of Held Synapse in a Mouse Model for Angelman Syndrome
The neurodevelopmental disorder Angelman syndrome (AS) is characterized by intellectual disability, motor dysfunction, distinct behavioral aspects, and epilepsy. AS is caused by a loss of the maternally expressed UBE3A gene, and many of the symptoms are recapitulated in a Ube3a mouse model of this s...
Na minha lista:
| Publicado no: | Front Cell Neurosci |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2018
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5758499/ https://ncbi.nlm.nih.gov/pubmed/29354033 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2017.00418 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|