| Name | Lysosomal Dysfunction in Progressive Supranuclear Palsy |
| Summary | Mechanistic overview of lysosomal dysfunction in PSP including autophagy-lysosome pathway impairment, cathepsin alterations, and therapeutic implications |
| Key Genes/Proteins | TREM2 p.Q33X mutation, TBK1 |
| Related Diseases | mitochondrial dysfunction, carcinoma, Alzheimer's disease, ALS, FTD |
| Related Pathways | TFEB activation |
| Linked Hypotheses | 1 hypotheses |