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US09090946B2 SE33 mutations impacting genotype concordance 有权
SE33突变影响基因型一致性

SE33 mutations impacting genotype concordance
摘要:
Disclosed are primer set compositions, methods and kits for human identification using the highly complex sequence locus, SE33 (ACTBP2) in single and multiplex PCR reactions. Additionally, disclosed are three newly discovered single nucleotide polymorphisms (SNPs) within the SE33 locus that can cause discordance seen as mobility shift or allelic dropout. Also disclosed are kits useful in human identification.
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