HFM1

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	Wikidata
View/Edit Human

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]

References

↑ ^1.0 ^1.1 Wang J, Zhang W, Jiang H, Wu BL (March 2014). "Mutations in HFM1 in recessive primary ovarian insufficiency". The New England Journal of Medicine. 370 (10): 972–4. doi:10.1056/NEJMc1310150. PMID 24597873.

[WangZhang2014-1] 1.0 ^1.1 Wang J, Zhang W, Jiang H, Wu BL (March 2014). "Mutations in HFM1 in recessive primary ovarian insufficiency". The New England Journal of Medicine. 370 (10): 972–4. doi:10.1056/NEJMc1310150. PMID 24597873.

[1]

HFM1

References

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