LRRK2gene variation and its contribution to Parkinson disease
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference100 articles.
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3. Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease;Berg;Brain,2005
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1. PAK6-mediated phosphorylation of PPP2R2C regulates LRRK2-PP2A complex formation;Frontiers in Molecular Neuroscience;2023-12-18
2. EndophilinA-dependent coupling between activity-induced calcium influx and synaptic autophagy is disrupted by a Parkinson-risk mutation;Neuron;2023-05
3. Genetic Evidence for Endolysosomal Dysfunction in Parkinson’s Disease: A Critical Overview;International Journal of Molecular Sciences;2023-03-28
4. EndophilinA-dependent coupling between activity-dependent calcium influx and synaptic autophagy is disrupted by a Parkinson-risk mutation;2022-04-30
5. High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic;Life;2022-01-14
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