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Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB.

Yufan WuYang LiGhulam MurtazaJianteng ZhouYuying JiaoChenjia GongCongyuan HuQiqi HanHuan ZhangYuanwei ZhangBaolu ShiHui MaXiaohua JiangQinghua Shi
Published in: Human reproduction (Oxford, England) (2021)
N/A.
Keyphrases
  • dna repair
  • genome wide
  • polycystic ovary syndrome
  • dna damage
  • type diabetes
  • insulin resistance
  • gene expression