Deficient Purposeful Use of Forepaws in Female Mice Modelling Rett Syndrome

Rett syndrome (RTT) is a rare neurodevelopmental disorder, characterized by severe behavioural and physiological symptoms. Mutations in the methyl CpG binding protein 2 gene (MECP2) cause more than 95% of classic cases. Motor abnormalities represent a significant part of the spectrum of RTT symptoms...

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Detalles Bibliográficos
Autores principales: De Filippis, Bianca, Musto, Mattia, Altabella, Luisa, Romano, Emilia, Canese, Rossella, Laviola, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491574/
https://www.ncbi.nlm.nih.gov/pubmed/26185689
http://dx.doi.org/10.1155/2015/326184

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491574/
https://www.ncbi.nlm.nih.gov/pubmed/26185689
http://dx.doi.org/10.1155/2015/326184

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