- Title
- A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next‐generation sequencing in a Chinese family
- Creators - without role
- Ru‐Qing Zhao - Panyu Hospital of Chinese MedicineFan Jiang - Guangzhou Medical UniversityJian Li - Guangzhou Women and Children Medical CenterJian‐Ying Zhou - Guangzhou Women and Children Medical CenterXue‐Wei Tang - Guangzhou Women and Children Medical CenterFa‐Tao Li - Guangzhou Women and Children Medical CenterLi‐Qiong Chen - Panyu Hospital of Chinese MedicineDong‐Zhi Li - Guangzhou Women and Children Medical CenterJianying Zhou - ISTD Pillar
- Publication Details
- International journal of laboratory hematology, Vol.43(6), pp.e294-e297
- Number of pages
- 4
- Identifiers
- 9911753209846
- Academic Unit
- ISTD Pillar
- Language
- English
- Resource Type
- Journal article
Journal article
A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next‐generation sequencing in a Chinese family
International journal of laboratory hematology, Vol.43(6), pp.e294-e297
12/2021
PMID: 33974364
Metrics
1 Record Views