Modulation of the GABAergic pathway for the treatment of fragile X syndrome

Fragile X syndrome (FXS) is the most common genetic cause of intellectual disability and the most common single-gene cause of autism. It is caused by mutations on the fragile X mental retardation gene (FMR1) and lack of fragile X mental retardation protein, which in turn, leads to decreased inhibiti...

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Detalles Bibliográficos
Autores principales: Lozano, Reymundo, Hare, Emma B, Hagerman, Randi J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172237/
https://www.ncbi.nlm.nih.gov/pubmed/25258535
http://dx.doi.org/10.2147/NDT.S42919

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172237/
https://www.ncbi.nlm.nih.gov/pubmed/25258535
http://dx.doi.org/10.2147/NDT.S42919

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