Abstract
In the past few years, mutations have been identified in the genes encoding alpha-synuclein, leucine-rich repeat kinase 2, and glucocerebrosidase in some patients with dementia with Lewy bodies (DLB). Furthermore, a novel locus for familial DLB has been mapped to chromosome 2q35-q36. Collectively, these discoveries highlight a substantial overlap between the known genetic determinants of Parkinson's disease and DLB, as well as the presence of profound etiologic heterogeneity in Lewy body disorders.
| Original language | Undefined/Unknown |
|---|---|
| Pages (from-to) | 187-189 |
| Number of pages | 3 |
| Journal | Current Neurology and Neuroscience Reports |
| Volume | 8 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 2008 |
Research programs
- EMC MGC-02-96-01
Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver