Loss of MeCP2 causes subtle alteration in dendritic arborization of retinal ganglion cells
Methyl-CpG-binding protein (MeCP2) is highly expressed in neurons. It plays an important role in the development of synapses and the formation of circuits in the central nervous system (CNS). Mutations in MECP2 cause neurodevelopmental disorders and mental retardation in humans. Therefore, it has be...
Guardat en:
| Autors principals: | , , , |
|---|---|
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Taylor & Francis Group
2021-03-01
|
| Col·lecció: | Animal Cells and Systems |
| Matèries: | |
| Accés en línia: | http://dx.doi.org/10.1080/19768354.2021.1920459 |
| Etiquetes: |
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|