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Analysis of known point mutations and SNPs in genes responsible for monogenic Parkinson’s disease in Russian patients
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作者 Elena V. Filatova Maria I. Shadrina +4 位作者 Ekaterina Y. Fedotova irina a. ivanova-smolenskaya Sergei N. Illarioshkin Svetlana A. Limborska Petr A. Slominsky 《Advances in Parkinson's Disease》 2013年第1期28-30,共3页
Background: Parkinson’s disease (PD) is caused by complex interactions between genetic and environmental factors. Mendelian forms of PD rarely occur in practice, but respective genes may play some role in pathogenesi... Background: Parkinson’s disease (PD) is caused by complex interactions between genetic and environmental factors. Mendelian forms of PD rarely occur in practice, but respective genes may play some role in pathogenesis of a common sporadic form of the disease. Methods: We analyzed most frequent known point mutations (PMs) and single-nucleotide polymorphisms (SNPs) in genes responsible for monogenic PD in 408 Russian patients, using arrayed primer extension (APEX), real-time PCR, and restriction fragment length polymorphism analysis. Results: We detected only three heterozygous PMs in the PARK2 gene in three non-related patients with early-onset sporadic PD. No association between PD and the studied SNPs was identified. Conclusion: The examined PMs and SNPs in genes responsible for monogenic PD do not contribute significantly to the development of sporadic PD in Russia. 展开更多
关键词 Parkinson’s Disease Point Mutations Single-Nucleotide POLYMORPHISMS
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