Neuroanatomical Phenotypes in a Mouse Model of the 22q11.2 Microdeletion

Recurrent deletions at the 22q11.2 locus have been established as a strong genetic risk factor for the development of schizophrenia and cognitive dysfunction. Individuals with 22q11.2 deletions have a range of well-defined volumetric abnormalities in a number of critical brain structures. A mouse mo...

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Detalhes bibliográficos
Main Authors: Ellegood, J., Markx, S., Lerch, J.P., Steadman, P.E., Genç, C., Provenzano, F, Kushner, S.A., Henkelman, R.M., Karayiorgou, M., Gogos, J.A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3872255/
https://ncbi.nlm.nih.gov/pubmed/23999526
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2013.112
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