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Neurological Sciences

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01-08-2011 | Letter to the Editor

A study of six point mutation analysis of LRRK2 gene in Chinese mainland patients with Parkinson’s disease

Authors: Z. X. Hu, D. T. Peng, M. Cai, J. L. Pu, X. G. Lei, X. Z. Yin, Z. Y. Ou-Yang, W. Luo, B. R. Zhang

Published in: Neurological Sciences | Issue 4/2011

Excerpt

Dear Editor, …

Thomas G (2009) Molecular pathogenesis of Parkinson disease: insights from genetic studies. Expert Rev Mol Med. doi:10.1077/S1462399409001148

Satake W, Nakabayashi Y, Mizuta I et al (2009) Genome-wide associated study identifies common variants at four loci as genetic risk factors for Parkinson’s disease. Nat Genet. doi:10.1038/ng.485

Pchelina SN, Yakimovskii AF, Emelyanov AK et al (2008) Screening for LRRK2 mutations in patients with Parkinson’s disease in Russia: identification of a novel LRRK2 variant. Eur J Neurol 15:692–696PubMedCrossRef

Lesage S, Ibanez P, Lohmann E et al (2005) G2019S LRRK2 mutation in French and North African families with Parkinson’s disease. Ann Neurol 58:784–787PubMedCrossRef

Lu CS, Simons EJ, Wu-Chou YH et al (2005) The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson’s disease. Parkinsonism Relat Disord 11:521–522PubMedCrossRef

Title: A study of six point mutation analysis of LRRK2 gene in Chinese mainland patients with Parkinson’s disease
Authors: Z. X. Hu
D. T. Peng
M. Cai
J. L. Pu
X. G. Lei
X. Z. Yin
Z. Y. Ou-Yang
W. Luo
B. R. Zhang
Publication date: 01-08-2011
Publisher: Springer Milan
Published in: Neurological Sciences / Issue 4/2011
Print ISSN: 1590-1874
Electronic ISSN: 1590-3478
DOI: https://doi.org/10.1007/s10072-010-0453-8

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A study of six point mutation analysis of LRRK2 gene in Chinese mainland patients with Parkinson’s disease

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