Mouse models of SYNGAP1-related intellectual disability

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SYNGAP1 is a Ras-GTPase activating protein highly enriched at excitatory synapses in the brain. De novo loss-of-function mutations in SYNGAP1 are a major cause of genetically defined neurodevelopmental disorders (NDD). These mutations are highly penetrant and cause SYNGAP1-related intellectual disab...

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Detalles Bibliográficos
Autores principales: Araki, Yoichi, Gerber, Elizabeth E., Rajkovich, Kacey E., Hong, Ingie, Johnson, Richard C., Lee, Hey-Kyoung, Kirkwood, Alfredo, Huganir, Richard L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245951/
https://www.ncbi.nlm.nih.gov/pubmed/37293116
http://dx.doi.org/10.1101/2023.05.25.542312

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245951/
https://www.ncbi.nlm.nih.gov/pubmed/37293116
http://dx.doi.org/10.1101/2023.05.25.542312

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