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The Fragile X Mutation Impairs Homeostatic Plasticity in Human Neurons by Blocking Synaptic Retinoic-Acid Signaling
Fragile X syndrome (FXS) is an X-chromosome-linked disease leading to severe intellectual disabilities. FXS is caused by inactivation of the fragile X mental retardation 1 (FMR1) gene, but how FMR1 inactivation induces FXS remains unclear. Using human neurons generated from control and FXS patient-d...
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| Publicat a: | Sci Transl Med |
|---|---|
| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6317709/ https://ncbi.nlm.nih.gov/pubmed/30068571 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/scitranslmed.aar4338 |
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