| Literature DB >> 28340952 |
Sun Ju Chung1, Mi-Jung Kim2, Ho-Sung Ryu3, Juyeon Kim4, Young Jin Kim3, Kiju Kim3, Sooyeoun You5, Seong Yoon Kim6, Jae-Hong Lee3.
Abstract
We investigated the role of mortalin (HSPA9) and its interaction with other mitochondria-related genes (parkin, PINK1, DJ1, and COQ2) as a risk factor for Parkinson's disease (PD) and Alzheimer's disease (AD) in 500 PD, 400 AD, and 500 control subjects. The HSPA9 variants identified by direct sequencing or its interaction with other genes assessed by genetic risk scores did not show a significant association with PD or AD risk. Our findings did not provide a strong evidence for the role of HAPA9 and its interaction with other mitochondria-related genes as a genetic risk factor for PD or AD.Entities:
Keywords: Alzheimer's disease; Genetic variation; Mitochondria; Parkinson's disease
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Year: 2016 PMID: 28340952 DOI: 10.1016/j.neurobiolaging.2016.09.017
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673