The I510V mutation in KLHL10 in a patient with oligoasthenoteratozoospermia

• Main Authors: Zicong HUANG (Author), Feilong CHEN (Author), Minyu XIE (Author), Hanbin ZHANG (Author), Yuge ZHUANG (Author), Chuyu HUANG (Author), Xuemei LI (Author), Hong LIU (Author), Zhenguo CHEN (Author)
• Format: Book
• Published: The Society for Reproduction and Development, 2021-08-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Oligoasthenoteratozoospermia is a human infertility syndrome caused by defects in spermatogenesis, spermiogenesis, and sperm maturation, and its etiology remains unclear. Kelch-like 10 (KLHL10) is a component of ubiquitin ligase E3 10 (KLHL10) and plays an important role in male fertility. Deletion...