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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: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | 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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