Mouse mutants in schizophrenia risk genes GRIN2A and AKAP11 show EEG abnormalities in common with schizophrenia patients

Schizophrenia is a heterogeneous psychiatric disorder with a strong genetic basis, whose etiology and pathophysiology remain poorly understood. Exome sequencing studies have uncovered rare, loss-of-function variants that greatly increase risk of schizophrenia [1], including loss-of-function mutation...

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Detalles Bibliográficos
Autores principales: Herzog, Linnea E., Wang, Lei, Yu, Eunah, Choi, Soonwook, Farsi, Zohreh, Song, Bryan J., Pan, Jen Q., Sheng, Morgan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10011509/
https://www.ncbi.nlm.nih.gov/pubmed/36914641
http://dx.doi.org/10.1038/s41398-023-02393-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10011509/
https://www.ncbi.nlm.nih.gov/pubmed/36914641
http://dx.doi.org/10.1038/s41398-023-02393-7

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