LRRK2 P755L variant in sporadic Parkinson’s disease-Reference-Cited by-同舟云学术

LRRK2 P755L variant in sporadic Parkinson’s disease

Published:2008-10-16 Issue:11-12 Volume:53 Page:1012-1015
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Tomiyama Hiroyuki,Mizuta Ikuko,Li Yuanzhe,Funayama Manabu,Yoshino Hiroyo,Li Lin,Murata Miho,Yamamoto Mitsutoshi,Kubo Shin-ichiro,Mizuno Yoshikuni,Toda Tatsushi,Hattori Nobutaka

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/jhg2008130.pdf

Reference17 articles.

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2. Di Fonzo A, Wu-Chou YH, Lu CS, van Doeselaar M, Simons EJ, Rohé CF, Chang HC, Chen RS, Weng YH, Vanacore N, Breedveld GJ, Oostra BA, Bonifati V (2006) A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan. Neurogenetics 7:133–138

3. Farrer MJ, Stone JT, Lin CH, Dächsel JC, Hulihan MM, Haugarvoll K, Ross OA, Wu RM (2007) Lrrk2 G2385R is an ancestral risk factor for Parkinson’s disease in Asia. Parkinsonism Relat Disord 13:89–92

4. Funayama M, Hasegawa K, Kowa H, Saito M, Tsuji S, Obata F (2002) A new locus for Parkinson’s disease (PARK8) maps to chromosome 12p11.2–q13.1. Ann Neurol 51:296–301

5. Funayama M, Li Y, Tomiyama H, Yoshino H, Imamichi Y, Yamamoto M, Murata M, Toda T, Mizuno Y, Hattori N (2007) Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population. NeuroReport 18:273–275

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