## Abstract Parkinson's disease (PD) is typically a sporadic illness, but the past decade has witnessed the identification of mutations responsible for multiple familial forms of the disease. The proposed functions of some of these genes (e.g., E3 ubiquitin ligase, redoxβdependent chaperone) have l
β¦ LIBER β¦
Gender differences in the risk of familial parkinsonism: Beyond LRRK2?
β Scribed by R. Saunders-Pullman; K. Stanley; M. San Luciano; M.J. Barrett; V. Shanker; D. Raymond; L.J. Ozelius; S.B. Bressman
- Book ID
- 116773128
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 136 KB
- Volume
- 496
- Category
- Article
- ISSN
- 0304-3940
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