Associated Papers
Identification of novel variants underlying non-syndromic primary ovarian insufficiency using a targeted NGS gene panel.
Veneziano C et al.
Frontiers in Endocrinology, 2025
41458559 (PubMed )
Supplement: Table4.xlsx › sheet1
Relationship between inhibin-α gene polymorphisms and premature ovarian failure in Korean women.
Kim H et al.
Menopause (new York, N.y.), 2011
Inhibin alpha-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers.
Longui CA et al.
Journal of Medical Genetics, 2004
How polymorphic markers contribute to genetic diseases in different populations? The study of inhibin A for premature ovarian insufficiency.
Christofolini DM et al.
Einstein (sao Paulo, Brazil), 0
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