A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
Key Points:
- Identification of aFTLD-U associated variants at chr15q14
- We performed a single variant GWAS using REGENIE7 comparing 59 neuropathologically confirmed aFTLD-U cases and 3,153 controls passing quality