Gender differences in the risk of familial parkinsonism: beyond LRRK2?

BACKGROUND: G2019S mutations in the LRRK2 gene are responsible for up to 18% of PD in individuals of Jewish descent. While a male preponderance of Parkinson disease (PD) has been consistently reported, this gender difference is not noted in LRRK2 G2019S mutation carriers. METHODS: In order to test w...

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Main Authors: Saunders-Pullman, R, Stanley, K, San Luciano, M, Barrett, MJ, Shanker, V, Raymond, D, Ozelius, LJ, Bressman, SB
格式: Artigo
語言:Inglês
出版: 2011
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3111955/
https://ncbi.nlm.nih.gov/pubmed/21511009
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2011.03.098
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