Open access
Jul 2026
Novel mutations in ZMYND15 expand the phenotypic spectrum to acephalic spermatozoa: abnormal sperm head-tail connection mediated by SUN5.
These mutations caused protein truncation and impaired function, leading to extremely low sperm counts, poor motility, and numerous acephalic spermatozoa, in ZMYND15 from two infertile patients.
Qian-Jun Zhang, Hao Lin, R. Hao et al.
· Asian Journal of Andrology · 0 citations