“Response to the letter to the editor “Concerns regarding the potentially causal role of FANCA heterozygous variants in human primary ovarian insufficiency””
Author:
Funder
National Key Research and Development Program of China
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-020-02233-4.pdf
Reference20 articles.
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2. Alvaro Mercadal B, Imbert R, Demeestere I, Gervy C, De Leener A, Englert Y, Costagliola S, Delbaere A (2015) AMH mutations with reduced in vitro bioactivity are related to premature ovarian insufficiency. Hum Reprod 30:1196–1202. https://doi.org/10.1093/humrep/dev042
3. Bouilly J, Beau I, Barraud S, Bernard V, Azibi K, Fagart J, Fèvre A, Todeschini AL, Veitia RA, Beldjord C, Delemer B, Dodé C, Young J, Binart N (2016) Identification of multiple gene mutations accounts for a new genetic architecture of primary ovarian insufficiency. J Clin Endocrinol Metabol 101:4541–4550. https://doi.org/10.1210/jc.2016-2152
4. Collins JK, Lane SIR, Merriman JA, Jones KT (2015) DNA damage induces a meiotic arrest in mouse oocytes mediated by the spindle assembly checkpoint. Nature Commun 6:8553. https://doi.org/10.1038/ncomms9553
5. Gurtan AM, Stuckert P, D’Andrea AD (2006) The WD40 repeats of FANCL are required for fanconi anemia core complex assembly. J Biol Chem 281:10896–10905
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