"Response to the letter to the editor "Concerns regarding the potentially causal role of FANCA heterozygous variants in human primary ovarian insufficiency""

Hum Genet. 2021 Apr;140(4):695-697. doi: 10.1007/s00439-020-02233-4. Epub 2020 Nov 11.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Fanconi Anemia Complementation Group A Protein / genetics
  • Female
  • Heterozygote
  • Humans
  • Primary Ovarian Insufficiency* / genetics

Substances

  • FANCA protein, human
  • Fanconi Anemia Complementation Group A Protein