Sign Up to like & get
recommendations!
2
Published in 2022 at "Movement Disorders"
DOI: 10.1002/mds.29144
Abstract: Loss‐of‐function mutations in GRN are a cause of familial frontotemporal dementia, and common variants within the gene have been associated with an increased risk of developing Alzheimer's disease and Parkinson's disease. Although TDP‐43‐positive inclusions are…
read more here.
Keywords:
associated lewy;
mutations associated;
grn mutations;
lewy body ... See more keywords