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Evidence for altered hippocampal function in a mouse model of the human 22q11.2 microdeletion

22q11.2 chromosomal deletions are recurrent copy number mutations that increase the risk of schizophrenia around thirty-fold. Deletion of the orthologous chromosomal region in mice offers an opportunity to characterize changes to neuronal structure and function that may account for the development o...

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Detalhes bibliográficos
Main Authors: Drew, Liam J, Stark, Kimberly L, Fénelon, Karine, Karayiorgou, Maria, MacDermott, Amy B, Gogos, Joseph A
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3539311/
https://ncbi.nlm.nih.gov/pubmed/21635953
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mcn.2011.05.008
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