(Q79555494)
Statements
Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants (English)
G M Hadjigeorgiou
V Gourbali
J Johnson
I Papakonstantinou
A Papadimitriou
A B Singleton
1 January 2007