Carrier Screening and Prenatal Diagnosis for Spinal Muscular Atrophy in Ningde City, Fujian Province
The frequency of SMA mutation in the Ningde area of Fujian province has been identified, which can provide the basis for genetic counseling and prenatal diagnosis. Interventional prenatal genetic diagnosis for high-risk fetuses can effectively prevent the birth of children with SMA and is crucial for preventing and controlling birth defects.
Authors
- Xiaomei Zeng (ORCID: https://orcid.org/0000-0001-5188-9944)
- WenXu Dong
- Xianguo Fu (ORCID: https://orcid.org/0000-0003-2116-2474)
- JiaoJiao Lu (ORCID: https://orcid.org/0000-0001-6568-7374)
- Xunyan Chen
- Xian Zheng
- Jing Yang (ORCID: https://orcid.org/0000-0001-7729-3452)
- Luoyuan Cao
- Qinjuan Wu
Institutions
- Fujian Medical University (CN)
- Ningde Normal University (CN)
Publication Details
- Journal
- Molecular Genetics & Genomic Medicine
- Published
- 2025-02-01
- DOI
- https://doi.org/10.1002/mgg3.70077
- Citations
- 2
- Primary Topic
- Neurogenetic and Muscular Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 3.25