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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...
Tallennettuna:
| Päätekijät: | , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2011
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| Aiheet: | |
| Linkit: | 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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