A homozygous mutation of TWNK identified in premature ovarian insufficiency warns of late-onset perrault syndrome-Reference-Cited by-同舟云学术

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A homozygous mutation of TWNK identified in premature ovarian insufficiency warns of late-onset perrault syndrome

Published:2024-08 Issue: Volume:299 Page:118-123
ISSN:0301-2115
Container-title:European Journal of Obstetrics & Gynecology and Reproductive Biology
language:en
Short-container-title:European Journal of Obstetrics & Gynecology and Reproductive Biology

Author:

Chang Xinyue,Li Guangyu,Fu Huimin,Guan Minxin,Guo Ting^ORCID

Publisher

Elsevier BV

Reference38 articles.

1. Primary ovarian insufficiency;Vos;Lancet,2010

2. Genetics of primary ovarian insufficiency: new developments and opportunities;Qin;Hum Reprod Update,2015

3. Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability;AlAsiri;J Clin Invest,2015

4. MCM9 Mutations Are Associated with Ovarian Failure, Short Stature, and Chromosomal Instability;Wood-Trageser;Am J Hum Genet,2014

5. Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans;Fan;Am J Hum Genet,2021

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