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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...

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Detalles Bibliográficos
Autores principales:	Lee, Wooje, Mariappan, Ramesh, De, Koushitak, Ohn, Takbum
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Taylor & Francis 2021
Materias:	Neurobiology & Physiology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8118406/ https://www.ncbi.nlm.nih.gov/pubmed/34234891 http://dx.doi.org/10.1080/19768354.2021.1920459

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