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Corticostriatal dysfunction underlies diminished striatal ascorbate release in the R6/2 mouse model of Huntington's disease

✍ Scribed by Jenelle L. Dorner; Benjamin R. Miller; Emma L. Klein; Alexander Murphy-Nakhnikian; Rachel L. Andrews; Scott J. Barton; George V. Rebec

No coin nor oath required. For personal study only.

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