Paternal Origin and Subsequent Maternal Inheritance of a Novel FOXL2 Frameshift Variant Underlie Accelerated Ovarian Aging: A Three-Generation BPES-I Family Study
Research Square
- FOXL2
- Blepharophimosis, ptosis, and epicanthus inversus syndrome
- Premature ovarian failure
- CYP19A1
- FST
- Humans
The paper
Li S, Hu M, Xu R et al.
Research Square · 28 Aug 2026 · Preprint, not peer-reviewed
