A novel heterozygous variant in PANX1 is associated with oocyte death and female infertility-Reference-Cited by-同舟云学术

A novel heterozygous variant in PANX1 is associated with oocyte death and female infertility

Published:2022-07-14 Issue:8 Volume:39 Page:1901-1908
ISSN:1058-0468
Container-title:Journal of Assisted Reproduction and Genetics
language:en
Short-container-title:J Assist Reprod Genet

Author:

Wu Xing-Wu,Liu Pei-Pei,Zou Yang,Xu Ding-Fei,Zhang Zhi-Qin,Cao Li-Yun,Lu-Fan ,Xia Lei-Zhen,Huang Jia-lv,Chen Jia,Xin Cai-Lin,Huang Zhi-Hui,Tan Jun^ORCID,Wu Qiong-Fang,Li Zeng-Ming

Funder

National Natural Science Foundation of China

Key Research and Development Program of Jiangxi Province

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Developmental Biology,Obstetrics and Gynecology,Genetics,Reproductive Medicine,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s10815-022-02566-1.pdf

Reference23 articles.

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2. Malizia BA, Hacker MR, Penzias AS. Cumulative live-birth rates after in vitro fertilization. N Engl J Med. 2009;360(3):236–43. https://doi.org/10.1056/NEJMoa0803072.

3. Smith A, Tilling K, Nelson SM, et al. Live-birth rate associated with repeat in vitro fertilization treatment cycles. JAMA. 2015;314(24):2654–62. https://doi.org/10.1001/jama.2015.17296.

4. Alazami AM, Awad SM, Coskun S, et al. TLE6 mutation causes the earliest known human embryonic lethality. Genome Biol. 2015;16:240. https://doi.org/10.1186/s13059-015-0792-0.

5. Chen B, Zhang Z, Sun X, et al. Biallelic mutations in PATL2 cause female infertility characterized by oocyte maturation arrest. Am J Hum Genet. 2017;101(4):609–15. https://doi.org/10.1016/j.ajhg.2017.08.018.

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1. A novel heterozygous missense variant of PANX1 causes human oocyte death and female infertility;Journal of Ovarian Research;2024-09-04

2. Genetic Causes of Oocyte-Based Infertility;Reference Module in Biomedical Sciences;2024

3. A novel heterozygous variant in PANX1 causes primary infertility due to oocyte death;Journal of Assisted Reproduction and Genetics;2022-12-05