Associated Papers
Identification of a missense variant of MND1 in meiotic arrest and non-obstructive azoospermia.
Zhao J et al.
Journal of Human Genetics, 2023
Ataxia with oculomotor apraxia type 2 caused by a novel homozygous mutation in SETX gene, and literature review.
Chen S et al.
Frontiers in Molecular Neuroscience, 2022
Select a paper to view details