Identification of a novel deletion mutation in DPY19L2 from an infertile patient with globozoospermia: a case report.
You-Zhu LiRong-Feng WuXing-Shen ZhuWen-Sheng LiuYuan-Yuan YeZhong-Xian LuNa LiPublished in: Molecular cytogenetics (2020)
The present study reported a male infertility patient who was diagnosed with globozoospermia. The analysis of gene mutations revealed that DPY19L2 had a homozygous mutation, which was the primary cause of globozoospermia.