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Published in 2022 at "Molecular biology of the cell"
DOI: 10.1091/mbc.p22-02-1003
Abstract: Loss-of-function mutations in VPS13C cause familial Parkinson’s disease (PD) and increase the risk to develop the sporadic form of the disease. However, the underlying disease mechanisms remain unclear. It has been previously established that VPS13C…
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Keywords:
transfer protein;
highlight lysosome;
lysosome lipid;
vps13c ... See more keywords