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Translation-relevant EEG phenotypes in a mouse model of Fragile X Syndrome
Identification of comparable biomarkers in humans and validated animal models will facilitate pre-clinical to clinical therapeutic pipelines to treat neurodevelopmental disorders. Fragile X Syndrome (FXS) is a leading known genetic cause of intellectual disability with symptoms that include increase...
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| Publicado en: | Neurobiol Dis |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5969806/ https://ncbi.nlm.nih.gov/pubmed/29605426 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2018.03.012 |
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