Compound heterozygous ZP1 mutations cause empty follicle syndrome in infertile sisters-Reference-Cited by-同舟云学术

Compound heterozygous ZP1 mutations cause empty follicle syndrome in infertile sisters

Published:2019-07-29 Issue:11 Volume:40 Page:2001-2006
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Sun Ling¹,Fang Xiang²,Chen Zhiheng¹,Zhang Hanwang³,Zhang Zhan²,Zhou Pei²,Xue Ting²,Peng Xiaofang²,Zhu Qianying²,Yin Minna¹,Liu Chunlin¹,Deng Yu¹,Hu Hao²,Li Na²^ORCID

Affiliation:

1. Center of Reproductive Medicine, Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou China

2. Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou China

3. Center of Reproductive Medicine, Tongji Medical College, Tongji Hospital Huazhong University of Science and Technology Wuhan China

Funder

Natural Science Foundation of Guangdong Province

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.23864

Reference22 articles.

1. A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility

2. Empty follicle syndrome

3. Empty follicle syndrome: Successful pregnancy following dual trigger

4. Double oocyte aspiration may be a solution for empty follicle syndrome: Case report

5. Integrated Sequence Analysis Pipeline Provides One-Stop Solution for Identifying Disease-Causing Mutations

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1. True empty follicle syndrome is a subtype of oocyte maturation abnormalities;Journal of Turkish Society of Obstetric and Gynecology;2024-09-04

2. ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans;Frontiers in Genetics;2024-06-20

3. Case report: A novel homozygous variant in ZP3 is associated with human empty follicle syndrome;Frontiers in Genetics;2023-10-16

4. A CASE REPORT OF A RARE NONSENSE ZP1 VARIANT IN A PATIENT WITH OOCYTE MATURATION DEFECT*;Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi;2023-07-25

5. Whole exome sequencing identifies a novel homozygous missense mutation of LHCGR gene in primary infertile women with empty follicle syndrome;Journal of Obstetrics and Gynaecology Research;2023-07-18