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Characterization of a mGluR5 Knockout Rat Model with Hallmarks of Fragile X Syndrome
The number of reported cases of neurodevelopmental disorders has increased significantly in the last few decades, but the etiology of these diseases remains poorly understood. There is evidence of a fundamental link between genetic abnormalities and symptoms of autism spectrum disorders (ASDs), and...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9504063/ https://www.ncbi.nlm.nih.gov/pubmed/36143345 http://dx.doi.org/10.3390/life12091308 |