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Functional Deficiencies in Fragile X Neurons Derived from Human Embryonic Stem Cells
Fragile X syndrome (FXS), the most common form of inherited mental retardation, is a neurodevelopmental disorder caused by silencing of the FMR1 gene, which in FXS becomes inactivated during human embryonic development. We have shown recently that this process is recapitulated by in vitro neural dif...
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| Pubblicato in: | J Neurosci |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Society for Neuroscience
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6605488/ https://ncbi.nlm.nih.gov/pubmed/26586818 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.0317-15.2015 |
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