The I510V mutation in KLHL10 in a patient with oligoasthenoteratozoospermia

• প্রধান লেখক: Zicong HUANG (লেখক), Feilong CHEN (লেখক), Minyu XIE (লেখক), Hanbin ZHANG (লেখক), Yuge ZHUANG (লেখক), Chuyu HUANG (লেখক), Xuemei LI (লেখক), Hong LIU (লেখক), Zhenguo CHEN (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: The Society for Reproduction and Development, 2021-08-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: 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...