VPS35 D620N knockin mice recapitulate cardinal features of Parkinson’s disease
VPS35 D620N knockin mice recapitulate cardinal features of Parkinson’s disease
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Publisher
England: John Wiley & Sons, Inc
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English
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Publisher
England: John Wiley & Sons, Inc
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D620N mutation in the vacuolar protein sorting 35 ortholog (VPS35) gene causes late‐onset, autosomal dominant familial Parkinson's disease (PD) and contributes to idiopathic PD. However, how D620N mutation leads to PD‐related deficits in vivo remains unclear. In the present study, we thoroughly characterized the biochemical, pathological, and behav...
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VPS35 D620N knockin mice recapitulate cardinal features of Parkinson’s disease
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8135078
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8135078
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ISSN
1474-9718
E-ISSN
1474-9726
DOI
10.1111/acel.13347
