TMEM106B a Novel Risk Factor for Frontotemporal Lobar Degeneration
Recently, the first genome-wide association (GWA) study in frontotemporal lobar degeneration (FTLD) identified common genetic variability at the TMEM106B gene on chromosome 7p21.3 as a potential important risk-modifying factor for FTLD with pathologic inclusions of TAR DNA-binding protein (FTLD-TDP)...
| Main Authors: | , |
|---|---|
| Format: | Online |
| Language: | English |
| Published: |
Humana Press Inc
2011
|
| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207134/ |