Response to “Should FANCL heterozygous pathogenic variants be considered as potentially causative of primary ovarian insufficiency?”-Reference-Cited by-同舟云学术

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Response to “Should FANCL heterozygous pathogenic variants be considered as potentially causative of primary ovarian insufficiency?”

Published:2020-08-26 Issue:9 Volume:41 Page:1700-1701
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Yang Yajuan¹²³⁴⁵,Zhao Shidou¹²³⁴⁵^ORCID,Qin Yingying¹²³⁴⁵^ORCID

Affiliation:

1. Center for Reproductive Medicine, Cheeloo College of Medicine Shandong University Jinan Shandong China

2. Key Laboratory of Reproductive Endocrinology of Ministry of Education Shandong University Jinan Shandong China

3. Shandong Key Laboratory of Reproductive Medicine Jinan Shandong China

4. Shandong Provincial Clinical Research Center for Reproductive Health Jinan Shandong China

5. National Research Center for Assisted Reproductive Technology and Reproductive Genetics Shandong University Jinan Shandong China

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24073

Reference19 articles.

1. Fanconi anemia and its diagnosis;Auerbach A. D.;Mutation Research/DNA Repair,2009

2. Homozygous hypomorphic BRCA2 variant in primary ovarian insufficiency without cancer or Fanconi anaemia trait

3. Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50

4. Minichromosome maintenance complex component 8 mutations cause primary ovarian insufficiency

5. A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice;Journal of Medical Genetics;2021-04-22

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