LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case–control association study for Parkinson's disease

BACKGROUND: The LRRK2 gene is associated with Parkinson's disease (PD) as a number of mutations within the gene have been shown to be susceptibility factors. Studies on various global populations have determined that mutations such as G2019S, G2385R, and R1628P in LRRK2 increase the risk of dev...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Mol Genet Genomic Med
Päätekijät: Gopalai, Aroma Agape, Lim, Jia Lun, Li, Hui‐Hua, Zhao, Yi, Lim, Thien Thien, Eow, Gaik B., Puvanarajah, Santhi, Viswanathan, Shanthi, Norlinah, Mohamed Ibrahim, Abdul Aziz, Zariah, Lim, Soo Kun, Tan, Chong Tin, Tan, Ai Huey, Lim, Shen‐Yang, Tan, Eng‐King, Ahmad Annuar, Azlina
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: John Wiley and Sons Inc. 2019
Aiheet:
Original Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6825847/
https://ncbi.nlm.nih.gov/pubmed/31487119
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.604
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