The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease

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Persistent URL	doi.org/10.1016/j.parkreldis.2005.09.003, hdl.handle.net/1765/52603
Journal	Parkinsonism & Related Disorders
Organisation	Department of Clinical Genetics
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Lu, C.-S., Simons, E., Wu-Chou, Y.-H., Di Fonzo, A., Chang, H.-C., Chen, R.-S., Weng, Y. H., Rohe, C. F., Breedveld, G., Hattori, N., Gasser, T., Oostra, B.& Bonifati, V. (2005). The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease. Parkinsonism & Related Disorders, 11(8), 521–522.https://doi.org/10.1016/j.parkreldis.2005.09.003

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