Identification of two compound heterozygous GNRHR mutations in two siblings with congenital hypogonadotropic hypogonadism

Asian J Androl. 2024 Jan 1;26(1):120-122. doi: 10.4103/aja20232. Epub 2023 Jun 16.
No abstract available

Publication types

  • Letter
  • Case Reports

MeSH terms

  • Adult
  • Female
  • Heterozygote*
  • Humans
  • Hypogonadism* / genetics
  • Male
  • Mutation*
  • Receptors, LHRH* / genetics
  • Siblings*

Substances

  • Receptors, LHRH
  • GNRHR protein, human