Whole exome sequencing identifies a novel mutation in Annexin A4 that is associated with recurrent spontaneous abortion
Our study suggests that an unreported novel <i>ANXA4</i> mutation (p.G8D) plays an important role in the pathogenesis of RSA and may contribute to the genetic diagnosis of RSA.
Authors
- Xiaojian Xia (ORCID: https://orcid.org/0000-0002-8140-9769)
- Faying Liu (ORCID: https://orcid.org/0000-0002-9922-2767)
- Li Zou (ORCID: https://orcid.org/0000-0003-4795-2343)
- Dandan Li (ORCID: https://orcid.org/0000-0003-2824-4130)
- Xiaoyong Chen (ORCID: https://orcid.org/0000-0002-4795-8940)
- Yang Zou (ORCID: https://orcid.org/0000-0002-7335-8850)
- Ying Cui (ORCID: https://orcid.org/0009-0006-0219-076X)
- Huimin Wu (ORCID: https://orcid.org/0000-0003-1012-6005)
- Ting Huang
- Qian Ye
- Chen-Nian Xia
Institutions
- Jiangxi University of Traditional Chinese Medicine (CN)
- Ganzhou People's Hospital (CN)
- Jiangxi Maternal and Child Health Hospital (CN)
Publication Details
- Journal
- Frontiers in Medicine
- Published
- 2024-09-27
- DOI
- https://doi.org/10.3389/fmed.2024.1462649
- Citations
- 2
- Primary Topic
- S100 Proteins and Annexins
- Type
- article
- Field-Weighted Citation Impact
- 0.47
Funders
- Natural Science Foundation of Jiangxi Province
- Key Research and Development Program of Jiangxi Province