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Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia.

Weili WangLilan SuLanlan MengJiaxin HeChen TanDuo YiDehua ChengHuan ZhangGuangxiu LuJuan DuGe LinQianjun ZhangChaofeng TuYue-Qiu Tan
Published in: Human reproduction (Oxford, England) (2023)
N/A.
Keyphrases
  • intellectual disability
  • copy number
  • polycystic ovary syndrome
  • type diabetes
  • autism spectrum disorder
  • gene expression
  • adipose tissue
  • metabolic syndrome
  • skeletal muscle
  • insulin resistance