Article
Granulin loss and TMEM106B risk converge on lysosomal C-terminal fragment pathology in frontotemporal dementia
2026-03-26
Abstract excerpt
Frontotemporal dementia (FTD) is the second most common cause of dementia after Alzheimer disease. Mutations in GRN , which encodes progranulin, are a major cause of FTD. Common genetic variants in the TMEM106B gene modify risk of FTD and the effect is especially strong in GRN mutation carriers. Intriguingly, in GRN mutation carriers, being homozygous for the protective TMEM106B haplotype seems to confer near...
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Identifiers and source
- Literature Corpus work
- f8e8f8b4-a219-5db8-be69-3b51a7e8f63c
- DOI
- 10.64898/2026.03.25.713523
