Clinical Characteristics and Gene Mutations of Hereditary Spherocytosis in 59 Chinese Children
We identified unique genetic and clinical characteristics mutations of HS in Chongqing, China. These findings expand the mutation spectrum of HS and have implications for early diagnosis and treatment of the disease.
Authors
- Xiao Li (ORCID: https://orcid.org/0000-0001-9785-4907)
- T. Y. Alvin Liu
- Yongjie Zhang (ORCID: https://orcid.org/0000-0003-3017-7838)
- Liang Huang (ORCID: https://orcid.org/0000-0003-3233-4446)
- Jie Yu (ORCID: https://orcid.org/0000-0001-5916-7073)
- Yan Xiang
- Yuzhuopu Li
- Yang Wang
Institutions
- Binzhou Medical University (CN)
- Binzhou Medical College Hospital (CN)
- Chengde Medical University (CN)
- Children's Hospital of Chongqing Medical University (CN)
- Chongqing Medical University (CN)
Publication Details
- Journal
- Molecular Genetics & Genomic Medicine
- Published
- 2026-02-21
- DOI
- https://doi.org/10.1002/mgg3.70188
- Primary Topic
- Erythrocyte Function and Pathophysiology
- Type
- article
- Field-Weighted Citation Impact
- 0.00