NeuroscienceNeurobiology of DiseasePeer-reviewed
Corticostriatal Maldevelopment in the R6/2 Mouse Model of Juvenile Huntington Disease
Carlos Cepeda, Sandra M. Holley, Joshua Barry…·Michael Levine
This paper examines corticostriatal development in the R6/2 mouse model of juvenile Huntington disease, finding early cortical malformations and transient synaptic deficits that normalize by postnatal day 21.
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