Mutations in the leucine rich repeat kinase 2 (LRRK2) gene are responsible for autosomal dominant and sporadic Parkinson disease (PD), possibly exerting their effects via a toxic gain of function. A common p.G2019S mutation (rs34637584:A>G) is responsible for up to 30-40% of PD cases in some ethnic
โฆ LIBER โฆ
Protection of peroxiredoxin II on oxidative stress-induced cardiomyocyte death and apoptosis
โ Scribed by Wen Zhao; Guo-Chang Fan; Zhi-Guo Zhang; Arun Bandyopadhyay; Xiaoyang Zhou; Evangelia G. Kranias
- Book ID
- 106067127
- Publisher
- Springer
- Year
- 2008
- Tongue
- English
- Weight
- 539 KB
- Volume
- 104
- Category
- Article
- ISSN
- 0300-8428
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