Loss-of-function mutation in TSGA10 causes acephalic spermatozoa phenotype in human.
Yuanyuan YeXiaoli WeiYanwei ShaNa LiXiaohong YanLing ChengDuanrui QiaoWeidong ZhouRongfeng WuQiaobin LiuYouzhu LiPublished in: Molecular genetics & genomic medicine (2020)
These results suggest that the novel homozygous frameshift insertion mutation of TSGA10 is a cause of acephalic spermatozoa.