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Comment
. 2022 Jan;21(1):22-23.
doi: 10.1016/S1474-4422(21)00411-7.

Development of treatments for Down syndrome

Affiliations
Comment

Development of treatments for Down syndrome

Michael S Rafii. Lancet Neurol. 2022 Jan.
No abstract available

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Comment on

References

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    1. Fernandez F, Morishita W, Zuniga E, et al. Pharmacotherapy for cognitive impairment in a mouse model of Down syndrome. Nat Neurosci 2007; 10: 411–13. - PubMed
    1. Kleschevnikov AM, Belichenko PV, Villar AJ, Epstein CJ, Malenka RC, Mobley WC. Hippocampal long-term potentiation suppressed by increased inhibition in the Ts65Dn mouse, a genetic model of Down syndrome. J Neurosci 2004; 24: 8153–60. - PMC - PubMed
    1. Scott-McKean JJ, Costa AC. Exaggerated NMDA mediated LTD in a mouse model of Down syndrome and pharmacological rescuing by memantine. Learn Mem 2011; 18: 774–78. - PMC - PubMed

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