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^*

^*Corresponding author for this work

Research output: Contribution to journal › Journal Letter › peer-review

74 Scopus citations

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
State	Published - 12 2005
Externally published	Yes

Access to Document

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

@article{6f4d40ae7cc047faa121b211af7b680d,

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

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",

year = "2005",

month = dec,

doi = "10.1016/j.parkreldis.2005.09.003",

language = "英语",

volume = "11",

pages = "521--522",

journal = "Parkinsonism and Related Disorders",

issn = "1353-8020",

publisher = "Elsevier Ltd",

number = "8",

}

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

TY - JOUR

T1 - The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease

AU - Lu, Chin Song

AU - Simons, Erik J.

AU - Wu-Chou, Yah Huei

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

AU - Gasser, Thomas

AU - Oostra, Ben A.

AU - Bonifati, Vincenzo

PY - 2005/12

Y1 - 2005/12

UR - http://www.scopus.com/inward/record.url?scp=27744446035&partnerID=8YFLogxK

U2 - 10.1016/j.parkreldis.2005.09.003

DO - 10.1016/j.parkreldis.2005.09.003

M3 - 快报

C2 - 16256409

AN - SCOPUS:27744446035

SN - 1353-8020

VL - 11

SP - 521

EP - 522

JO - Parkinsonism and Related Disorders

JF - Parkinsonism and Related Disorders

IS - 8

ER -

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

Access to Document

Other files and links

Cite this