Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6284045 | Neuroscience Letters | 2012 | 4 Pages |
Abstract
⺠Mutation of GBA, a causative gene for Gaucher disease is rare in Asia. ⺠We analyzed mutations in GBA in 277 Korean PD and 291 controls. ⺠Heterozygous mutation of GBA was found in 3.2% of PD cases and 0% in controls. ⺠Age-at-onset was younger in heterozygous GBA mutation carriers than non-carriers.
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Authors
Jung Mi Choi, Won Chan Kim, Chul Hyoung Lyoo, Suk Yun Kang, Phil Hyu Lee, Jong Sam Baik, Seong-Beom Koh, Hyeo-Il Ma, Young Ho Sohn, Myung Sik Lee, Yun Joong Kim,