A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency
- Faculté de médecine Paris Sud, France
- Université Paris Sud, France
- Université Paris Diderot, France
- Turku University Hospital, Finland
- Hôpital Necker-enfants malades, APHP, France
- Faculté de Médecine Laennec, France
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A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency
eLife 6:e30490.
https://doi.org/10.7554/eLife.30490
