Discovery of a rare genotype causing primary ovarian insufficiency
Scientists at deCODE genetics and collaborators, have identified a sequence variant in the CCDC201 gene that when inherited from both parents homozygous causes menopause on average nine years earlier. deCODE genetics, a subsidiary of Amgen, and collaborators from Iceland, Denmark, the UK, and Norway published a study in Nature Genetics today revealing a rare genotype with a significant impact on women's health. Age at menopause significantly affects fertility and disease risk. This research focused on ...
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