FANCL gene mutations in premature ovarian insufficiency-Reference-Cited by-同舟云学术

FANCL gene mutations in premature ovarian insufficiency

Published:2020-02-24 Issue:5 Volume:41 Page:1033-1041
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Yang Yajuan¹,Guo Ting¹,Liu Ran¹,Ke Hanni¹,Xu Weiwei¹,Zhao Shidou¹^ORCID,Qin Yingying¹^ORCID

Affiliation:

1. Center for Reproductive Medicine, Key Laboratory of Reproductive Endocrinology of Ministry of Education, National Research Center for Assisted Reproductive Technology and Reproductive GeneticsShandong University Jinan Shandong China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.23997

Reference36 articles.

1. A novel gene, Pog, is necessary for primordial germ cell proliferation in the mouse and underlies the germ cell deficient mutation, gcd

2. Identification and characterization of mutations in FANCL gene: A second case of Fanconi anemia belonging to FA-L complementation group

3. Mechanistic Insight into Site-Restricted Monoubiquitination of FANCD2 by Ube2t, FANCL, and FANCI

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

5. Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells;Ceccaldi R.;Cell Stem Cell,2012

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