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BackgroundSingle‐nucleotide polymorphisms (SNPs) have been reported as a highly relevant point for the mechanisms of Parkinson's disease (PD). The invention of saturating dye makes it possible to identify heteroduplex DNA without redistribution during melting, which allows using high‐resolution melting (HRM) to detect SNPs. However, the HRM analysis for detection of those SNPs associated with PD was...
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