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Familial genes in sporadic disease: Common variants of α-Synuclein gene associate with Parkinson’s disease
Genetic variation of the α-synuclein gene (SNCA) is known to cause familial parkinsonism, however the role of SNCA variants in sporadic Parkinson’s disease (PD) remains elusive. The present study identifies an association of common SNCA polymorphisms with disease susceptibility in a series of Irish...
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| Главные авторы: | , , , , , , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2007
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2970620/ https://ncbi.nlm.nih.gov/pubmed/17531291 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mad.2007.04.002 |
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