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Genetic association study of a single nucleotide polymorphism of kallikrein-related peptidase 2 with male infertility
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  • Genetic association study of a single nucleotide polymorphism of kallikrein-related peptidase 2 with male infertility
  • Genetic association study of a single nucleotide polymorphism of kallikrein-related peptidase 2 with male infertility
저자명
Lee. Sun-Hee,Lee. Su-Man
간행물명
Clinical and experimental reproductive medicine
권/호정보
2011년|38권 1호|pp.6-9 (4 pages)
발행정보
대한생식의학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Objective: To investigate a kallikrein-related peptidase 2 (KLK2) single nucleotide polymorphism (SNP) in relation to male infertility because of its role in semen processing. We investigated the genetic association of the KLK2+255G>A genotype with male infertility. Methods: We genotyped the SNP site located in intron 1 (+255G>A, rs2664155) of KLK2 from 218 men with male infertility (cases) and 220 fertile males (controls). Pyrosequencing analysis was performed for the genotyping. Results: The SNP of the KLK2 gene had a statistically significant association with male infertility (p<0.05). The odds ratio for the minor allele (+255A) in the pooled sample was 0.47 (95% confidence intervals, 0.26-0.85) for rs2664155. Conclusion: The relationship of KLK2 SNP to male infertility is statistically significant, especially within the non-azoospermia group. Further study is needed to understand the mechanisms associated with male infertility.