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The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease
P1-309
Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease
Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease
A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly
