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

Chin Song Lu; Erik J. Simons; Yah Huei Wu-Chou; Alessio Di Fonzo; Hsiu Chen Chang; Rou Shayn Chen; Yi Hsin Weng; Christan F. Rohé; Guido J. Breedveld; Nobutaka Hattori; Thomas Gasser; Ben A. Oostra; Vincenzo Bonifati

doi:10.1016/j.parkreldis.2005.09.003

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

Chin Song Lu, Erik J. Simons, Yah Huei Wu-Chou, Alessio Di Fonzo, Hsiu Chen Chang, Rou Shayn Chen, Yi Hsin Weng, Christan F. Rohé, Guido J. Breedveld, Nobutaka Hattori, Thomas Gasser, Ben A. Oostra, Vincenzo Bonifati

Fondazione IRCCS Ca' Granda- Ospedale Maggiore Policlinico

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	521-522
Number of pages	2
Journal	Parkinsonism and Related Disorders
Volume	11
Issue number	8
DOIs	https://doi.org/10.1016/j.parkreldis.2005.09.003
Publication status	Published - Dec 2005

ASJC Scopus subject areas

Ageing
Clinical Neurology
Neurology

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10.1016/j.parkreldis.2005.09.003

Cite this

Lu, C. S., Simons, E. J., Wu-Chou, Y. H., Fonzo, A. D., Chang, H. C., Chen, R. S., Weng, Y. H., Rohé, C. F., Breedveld, G. J., Hattori, N., Gasser, T., Oostra, B. A., & Bonifati, V. (2005). The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease. Parkinsonism and Related Disorders, 11(8), 521-522. https://doi.org/10.1016/j.parkreldis.2005.09.003

The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease. / Lu, Chin Song; Simons, Erik J.; Wu-Chou, Yah Huei; Fonzo, Alessio Di; Chang, Hsiu Chen; Chen, Rou Shayn; Weng, Yi Hsin; Rohé, Christan F.; Breedveld, Guido J.; Hattori, Nobutaka; Gasser, Thomas; Oostra, Ben A.; Bonifati, Vincenzo.

In: Parkinsonism and Related Disorders, Vol. 11, No. 8, 12.2005, p. 521-522.

Research output: Contribution to journal › Article › peer-review

Lu, CS, Simons, EJ, Wu-Chou, YH, Fonzo, AD, Chang, HC, Chen, RS, Weng, YH, Rohé, CF, Breedveld, GJ, Hattori, N, Gasser, T, Oostra, BA & Bonifati, V 2005, 'The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease', Parkinsonism and Related Disorders, vol. 11, no. 8, pp. 521-522. https://doi.org/10.1016/j.parkreldis.2005.09.003

Lu, Chin Song ; Simons, Erik J. ; Wu-Chou, Yah Huei ; Fonzo, Alessio Di ; Chang, Hsiu Chen ; Chen, Rou Shayn ; Weng, Yi Hsin ; Rohé, Christan F. ; Breedveld, Guido J. ; Hattori, Nobutaka ; Gasser, Thomas ; Oostra, Ben A. ; Bonifati, Vincenzo. / The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease. In: Parkinsonism and Related Disorders. 2005 ; Vol. 11, No. 8. pp. 521-522.

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author = "Lu, {Chin Song} and Simons, {Erik J.} and Wu-Chou, {Yah Huei} and Fonzo, {Alessio Di} and Chang, {Hsiu Chen} and Chen, {Rou Shayn} and Weng, {Yi Hsin} and Roh{\'e}, {Christan F.} and Breedveld, {Guido J.} and Nobutaka Hattori and Thomas Gasser and Oostra, {Ben A.} and Vincenzo Bonifati",

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AU - Fonzo, Alessio Di

AU - Chang, Hsiu Chen

AU - Chen, Rou Shayn

AU - Weng, Yi Hsin

AU - Rohé, Christan F.

AU - Breedveld, Guido J.

AU - Hattori, Nobutaka

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AU - Oostra, Ben A.

AU - Bonifati, Vincenzo

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