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...

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Detalles Bibliográficos
Autores principales: Dahl, Victoria, Helmbrecht, Hawley, Rios Sigler, Ana, Hildahl, Kate, Sullivan, Holly, Janakiraman, Sanjana, Jasti, Saahiti, Nance, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9504063/
https://www.ncbi.nlm.nih.gov/pubmed/36143345
http://dx.doi.org/10.3390/life12091308

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