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Ben A Oostra
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Works
6
The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease
scientific article published on 26 October 2005
P1-309
Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil
scientific article published on 22 November 2005
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease
scientific article published on February 16, 2012
Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease
scientific article published on March 24, 2012
A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly
scientific article (publication date: 15 July 2003)
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