
07/25/2025
FTD Fact Friday: Heterozygous loss-of-function mutations in GRN are the second most common cause of inherited FTLD-TDP. The Penn FTD Center is here to help with information and resources!
📍 Check out our Support & Resources tab for helpful tools and links.
đź“° Read our monthly blog in the Latest News tab.
🔎 Interested in Observational Research or Clinical Trials? Click the links to learn more about the participation in studies.
Find more information on the Penn FTD Center website!