HFM1 explained

HFM1 is a gene that in humans encodes a protein necessary for homologous recombination of chromosomes.^[1] Biallelic mutations in HFM1 cause recessive primary ovarian insufficiency.^[1]

Notes and References

1. Wang J, Zhang W, Jiang H, Wu BL . Mutations in HFM1 in recessive primary ovarian insufficiency . The New England Journal of Medicine . 370 . 10 . 972–4 . March 2014 . 24597873 . 10.1056/NEJMc1310150 . free .