Associated Papers
A homozygous missense variant in YTHDC2 induces azoospermia in two siblings.
Tian S et al.
Molecular Genetics and Genomics : Mgg, 2024
Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiency.
McGlacken-Byrne SM et al.
Jci Insight, 2022
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