Abstract
BACKGROUND: Mutations in the gene Leucine-Rich Repeat Kinase 2 (LRRK2) were recently identified as the cause of PARK8 linked autosomal dominant Parkinson's disease. OBJECTIVE: To study recurrent LRRK2 mutations in a large sample of patients from Italy, including early (
Original language | English |
---|---|
Journal | Journal of Medical Genetics |
Volume | 42 |
Issue number | 11 |
Publication status | Published - Nov 2005 |
ASJC Scopus subject areas
- Genetics
- Genetics(clinical)