A homozygous loss‐of‐function mutation in FBXO43 causes human non‐obstructive azoospermia-Reference-Cited by-同舟云学术

A homozygous loss‐of‐function mutation in FBXO43 causes human non‐obstructive azoospermia

Published:2021-10-11 Issue:1 Volume:101 Page:55-64
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Wu Huan¹²³^ORCID,Zhang Xin⁴,Shen Qunshan¹⁵⁶,Liu Yiyuan¹,Gao Yang¹⁵⁶^ORCID,Wang Guanxiong¹,Lv Mingrong¹⁵⁶,Hua Rong⁴,Xu Yuping¹⁵⁶,Zhou Ping¹⁵⁶,Wei Zhaolian¹⁵⁶,Tao Fangbiao²³,He Xiaojin¹²³^ORCID,Cao Yunxia¹²³,Liu Mingxi⁴

Affiliation:

1. Reproductive Medicine Center, Department of Obstetrics and Gynecology The First Affiliated Hospital of Anhui Medical University Hefei China

2. NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract Anhui Medical University Hefei China

3. Key Laboratory of Population Health Across Life Cycle (Anhui Medical University) Ministry of Education of the People's Republic of China Hefei China

4. State Key Laboratory of Reproductive Medicine, Department of Histology and Embryology School of Basic Medical Sciences, Nanjing Medical University Nanjing China

5. Anhui Province Key Laboratory of Reproductive Health and Genetics Anhui Medical University Hefei China

6. Biopreservation and Artificial Organs Anhui Provincial Engineering Research Center, Anhui Medical University Hefei China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Anhui Province

Natural Science Foundation of Jiangsu Province

Qinglan Project of Jiangsu Province of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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