MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats

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Since the identification of MECP2 as the causative gene in the majority of Rett Syndrome (RTT) cases, transgenic mouse models have played a critical role in our understanding of this disease. The use of additional mammalian RTT models offers the promise of further elucidating critical early mechanis...

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Detalles Bibliográficos
Autores principales: Patterson, Kelsey C., Hawkins, Virginia E., Arps, Kara M., Mulkey, Daniel K., Olsen, Michelle L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179928/
https://www.ncbi.nlm.nih.gov/pubmed/27329765
http://dx.doi.org/10.1093/hmg/ddw179

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