Carregant...
Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release
Heterozygous mutations of the Forkhead-box protein 2 (FOXP2) gene in humans cause childhood apraxia of speech. Loss of Foxp2 in mice is known to affect striatal development and impair motor skills. However, it is unknown if striatal excitatory/inhibitory balance is affected during development and if...
Guardat en:
| Publicat a: | Brain Struct Funct |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Berlin Heidelberg
2018
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6267273/ https://ncbi.nlm.nih.gov/pubmed/30187194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00429-018-1746-6 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|