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

CS Lu; Erik Simons; YH Wu-Chou; Alessio Di Fonzo; HC Chang; RS Chen; YH Weng; Christan Rohe; Guido Breedveld; N Hattori; T Gasser; Ben 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

CS Lu, Erik Simons, YH Wu-Chou, Alessio Di Fonzo, HC Chang, RS Chen, YH Weng, Christan Rohe, Guido Breedveld, N Hattori, T Gasser, Ben Oostra, Vincenzo Bonifati

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

74 Citations (Scopus)

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

Research programs

EMC MGC-02-96-01

Access to Document

10.1016/j.parkreldis.2005.09.003

http://hdl.handle.net/1765/52603

Cite this

Lu, CS., Simons, E., Wu-Chou, YH., Di Fonzo, A., Chang, HC., Chen, RS., Weng, YH., Rohe, C., 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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title = "The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease",

author = "CS Lu and Erik Simons and YH Wu-Chou and {Di Fonzo}, Alessio and HC Chang and RS Chen and YH Weng and Christan Rohe and Guido Breedveld and N Hattori and T Gasser and Ben Oostra and Vincenzo Bonifati",

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

language = "Undefined/Unknown",

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pages = "521--522",

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Lu, CS, Simons, E, Wu-Chou, YH, Di Fonzo, A, Chang, HC, Chen, RS, Weng, YH, Rohe, C, 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, 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, CS

AU - Simons, Erik

AU - Wu-Chou, YH

AU - Di Fonzo, Alessio

AU - Chang, HC

AU - Chen, RS

AU - Weng, YH

AU - Rohe, Christan

AU - Breedveld, Guido

AU - Hattori, N

AU - Gasser, T

AU - Oostra, Ben

AU - Bonifati, Vincenzo

PY - 2005

Y1 - 2005

U2 - 10.1016/j.parkreldis.2005.09.003

DO - 10.1016/j.parkreldis.2005.09.003

M3 - Article

SN - 1353-8020

VL - 11

SP - 521

EP - 522

JO - Parkinsonism & Related Disorders

JF - Parkinsonism & Related Disorders

IS - 8

ER -