The I510V mutation in <i>KLHL10</i> in a patient with oligoasthenoteratozoospermia-Reference-Cited by-同舟云学术

The I510V mutation in KLHL10 in a patient with oligoasthenoteratozoospermia

Published:2021 Issue:5 Volume:67 Page:313-318
ISSN:0916-8818
Container-title:Journal of Reproduction and Development
language:en
Short-container-title:Journal of Reproduction and Development

Author:

HUANG Zicong¹,CHEN Feilong²,XIE Minyu¹,ZHANG Hanbin¹,ZHUANG Yuge¹,HUANG Chuyu³,LI Xuemei⁴,LIU Hong⁴,CHEN Zhenguo¹

Affiliation:

1. Department of Cell Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, P. R. China

2. Department of Pathology, Panyu Maternal and Child Care Service Centre of Guangzhou, Guangzhou 511499, P. R. China

3. Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China

4. Reproductive center, Affiliated Shenzhen Maternity & Child Healthcare Hospital, Southern Medical University (Shenzhen Maternity & Child Healthcare Hospital), Shenzhen 518017, P. R. China

Publisher

Japanese Society of Animal Reproduction

Subject

Animal Science and Zoology

Link

https://www.jstage.jst.go.jp/article/jrd/67/5/67_2021-063/_pdf

Reference22 articles.

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2. 2. Zorrilla M, Yatsenko AN. The genetics of infertility: current status of the field. Curr Genet Med Rep 2013; 1: 247–260.

3. 3. O’Flynn O’Brien KL, Varghese AC, Agarwal A. The genetic causes of male factor infertility: a review. Fertil Steril 2010; 93: 1–12.

4. 4. Chu DS, Shakes DC. Spermatogenesis. Adv Exp Med Biol 2013; 757: 171–203.

5. 5. Gadella BM, Luna C. Cell biology and functional dynamics of the mammalian sperm surface. Theriogenology 2014; 81: 74–84.

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1. Homozygous frameshift variant in POC1B causes male infertility with oligoasthenoteratozoospermia in human and mice;Human Molecular Genetics;2023-04-18

2. A novel loss-of-function variant in PNLDC1 inducing oligo-astheno-teratozoospermia and male infertility;Asian Journal of Andrology;2023

3. BiallelicCFAP61variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia;Journal of Medical Genetics;2022-04-06