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Progress toward therapeutic potential for AFQ056 in Fragile X syndrome
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and the leading single-gene cause of autism. It is caused by the lack of production of the Fragile X mental retardation protein (FMRP), resulting in cognitive deficits, hyperactivity, and autistic behaviors. Breakt...
Sparad:
| I publikationen: | J Exp Pharmacol |
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| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Dove Medical Press
2013
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4863540/ https://ncbi.nlm.nih.gov/pubmed/27186135 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/JEP.S27044 |
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