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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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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Dove Medical Press
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4172237/ https://ncbi.nlm.nih.gov/pubmed/25258535 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/NDT.S42919 |
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