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Discovery of a rare genotype causing primary ovarian insufficiency 

Aug 27, 2024 | NEWS

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.  Kari Stefansson, Patrick Sulem and Asmundur Oddsson authors...

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deCODE genetics | Sturlugata 8 | 101 Reykjavik | Iceland | phone +354 570 1900