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Alterations in CA1 hippocampal synapses in a mouse model of Fragile X Syndrome
Fragile X Syndrome (FXS) is the major cause of inherited mental retardation and the leading genetic cause of Autism Spectrum Disorders (ASDs). FXS is caused by mutations in the Fragile X Mental Retardation 1 (Fmr1) gene, which results in transcriptional silencing of Fragile X Mental Retardation Prot...
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| Publicado no: | Glia |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5812820/ https://ncbi.nlm.nih.gov/pubmed/29274095 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/glia.23284 |
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