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Lack of association between the LRRK2 A419V variant and Asian Parkinson's disease.
Gopalai AA, Lim SY, Aziz ZA, Lim SK, Tan LP, Chong YB, Tan CT, Puvanarajah S, Viswanathan S, Kuppusamy R, Tan AH, Lim TT, Eow GB, Norlinah MI, Li HH, Zhao Y, Ahmad-Annuar A. Gopalai AA, et al. Among authors: lim sy, lim tt, lim sk. Ann Acad Med Singap. 2013 May;42(5):237-40. Ann Acad Med Singap. 2013. PMID: 23771111 Free article.
LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian population.
Gopalai AA, Lim SY, Chua JY, Tey S, Lim TT, Mohamed Ibrahim N, Tan AH, Eow GB, Abdul Aziz Z, Puvanarajah SD, Viswanathan S, Looi I, Lim SK, Tan LP, Chong YB, Tan CT, Zhao Y, Tan EK, Ahmad-Annuar A. Gopalai AA, et al. Among authors: lim sy, lim tt, lim sk. Biomed Res Int. 2014;2014:867321. doi: 10.1155/2014/867321. Epub 2014 Aug 28. Biomed Res Int. 2014. PMID: 25243190 Free PMC article.
PARK16 is associated with PD in the Malaysian population.
Gopalai AA, Ahmad-Annuar A, Li HH, Zhao Y, Lim SY, Tan AH, Lim TT, Eow GB, Santhi P, Shanthi V, Norlinah MI, Aziz ZA, Lim SK, Tan CT, Tan EK. Gopalai AA, et al. Among authors: lim sy, lim tt, lim sk. Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):839-47. doi: 10.1002/ajmg.b.32454. Epub 2016 May 13. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 27174169
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case-control association study for Parkinson's disease.
Gopalai AA, Lim JL, Li HH, Zhao Y, Lim TT, Eow GB, Puvanarajah S, Viswanathan S, Norlinah MI, Abdul Aziz Z, Lim SK, Tan CT, Tan AH, Lim SY, Tan EK, Ahmad Annuar A. Gopalai AA, et al. Among authors: lim sy, lim tt, lim jl, lim sk. Mol Genet Genomic Med. 2019 Nov;7(11):e604. doi: 10.1002/mgg3.604. Epub 2019 Sep 5. Mol Genet Genomic Med. 2019. PMID: 31487119 Free PMC article.
1,058 results