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
Molecular functions of MCM8 and MCM9 and their associated pathologies.
Helderman NC et al.
Iscience, 2023
Structural study of the N-terminal domain of human MCM8/9 complex.
Li J et al.
Structure (london, England : 1993), 2021
Germline biallelic Mcm8 variants are associated with early-onset Lynch-like syndrome.
Golubicki M et al.
Jci Insight, 2020
MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency.
Desai S et al.
The Journal of Clinical Endocrinology and Metabolism, 2017
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1871.656
Select a paper to view details