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Am J Med Genet B

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GBA gene mutations cause dysfunction of the autophagy-lysosome pathway and reduced glucocerebrosidase (GCase) activity [21], resulting in -syn aggregation and OS

Renin-angiotensin-aldosterone system inhibition: overview of the therapeutic use of angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, mineralocorticoid receptor antagonists, and direct renin inhibitors

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