Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice

Conclusion
Our findings prove for the first time that defects in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans.

Source: Journal of Medical Genetics - January 24, 2023 Category: Genetics & Stem Cells Authors: Liu, W., Wei, X., Liu, X., Chen, G., Zhang, X., Liang, X., Isachenko, V., Sha, Y., Wang, Y. Tags: Gametes Source Type: research