Recent advances in the genetics of dementia with Lewy bodies

Research output: Contribution to journalArticleAcademic

18 Citations (Scopus)

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 languageUndefined/Unknown
Pages (from-to)187-189
Number of pages3
JournalCurrent Neurology and Neuroscience Reports
Volume8
Issue number3
DOIs
Publication statusPublished - 2008

Research programs

  • EMC MGC-02-96-01

Cite this