Associated Papers
Clinical syndromes linked to biallelic germline variants in MCM8 and MCM9.
Helderman NC et al.
Hgg Advances, 2025
40684266 (PubMed )
Supplement: mmc1.pdf
Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency.
Zhang YX et al.
Molecular Genetics & Genomic Medicine, 2020
MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency.
Desai S et al.
The Journal of Clinical Endocrinology and Metabolism, 2017
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