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NRXN1α(+/-) is associated with increased excitability in ASD iPSC-derived neurons
BACKGROUND: NRXN1 deletions are identified as one of major rare risk factors for autism spectrum disorder (ASD) and other neurodevelopmental disorders. ASD has 30% co-morbidity with epilepsy, and the latter is associated with excessive neuronal firing. NRXN1 encodes hundreds of presynaptic neuro-adh...
Autores principales: | Avazzadeh, Sahar, Quinlan, Leo R., Reilly, Jamie, McDonagh, Katya, Jalali, Amirhossein, Wang, Yanqin, McInerney, Veronica, Krawczyk, Janusz, Ding, Yicheng, Fitzgerald, Jacqueline, O’Sullivan, Matthew, Forman, Eva B., Lynch, Sally A., Ennis, Sean, Feerick, Niamh, Reilly, Richard, Li, Weidong, Shen, Xu, Yang, Guangming, Lu, Yin, Peeters, Hilde, Dockery, Peter, O’Brien, Timothy, Shen, Sanbing, Gallagher, Louise |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8442436/ https://www.ncbi.nlm.nih.gov/pubmed/34525970 http://dx.doi.org/10.1186/s12868-021-00661-0 |
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