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Published in 2023 at "ACS chemical neuroscience"
DOI: 10.1021/acschemneuro.2c00466
Abstract: Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the common causes of inherited Parkinson's disease (PD) and emerged as a causative PD gene. Particularly, LRRK2-Gly2019Ser mutation was reported to alter the early phase…
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Keywords:
evaluation 18f;
brain;
lrrk2;
18f 06455943 ... See more keywords