Ładuje się......
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...
Zapisane w:
| Wydane w: | Brain Struct Funct |
|---|---|
| Główni autorzy: | , , , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
Springer Berlin Heidelberg
2018
|
| Hasła przedmiotowe: | |
| Dostęp online: | 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 |
| Etykiety: |
Dodaj etykietę
Nie ma etykietki, Dołącz pierwszą etykiete!
|