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CHD7 missense variants and clinical characteristics of Chinese males with infertility.

Leilei LiRuixue WangYang YuHongguo ZhangYuting JiangXiao YangRuizhi Liu
Published in: Molecular genetics & genomic medicine (2020)
There may be a relationship between the CHD7 gene missense variants and male infertility. These variants are easier to find in patients with azoospermia and severe oligospermia whose testosterone levels are decreased.
Keyphrases
  • copy number
  • intellectual disability
  • genome wide
  • polycystic ovary syndrome
  • early onset
  • skeletal muscle
  • genome wide identification