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Published in 2020 at "Neurobiology of Disease"
DOI: 10.1016/j.nbd.2020.104737
Abstract: Loss-of-function mutations in the parkin-encoding PARK2 gene are a frequent cause of young-onset, autosomal recessive Parkinson's disease (PD). Parkin knockout mice have no nigro-striatal neuronal loss but exhibit abnormalities of striatal dopamine transmission and cortico-striatal…
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Keywords:
circuit dynamics;
deficiency perturbs;
parkin deficiency;
circuit ... See more keywords