Alterations of in vivo CA1 network activity in Dp(16)1Yey Down syndrome model mice
Down syndrome, the leading genetic cause of intellectual disability, results from an extra-copy of chromosome 21. Mice engineered to model this aneuploidy exhibit Down syndrome-like memory deficits in spatial and contextual tasks. While abnormal neuronal function has been identified in these models,...
Main Authors: | Matthieu Raveau, Denis Polygalov, Roman Boehringer, Kenji Amano, Kazuhiro Yamakawa, Thomas J McHugh |
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Format: | Article |
Language: | English |
Published: |
eLife Sciences Publications Ltd
2018-02-01
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Series: | eLife |
Subjects: | |
Online Access: | https://elifesciences.org/articles/31543 |
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