Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report
- DOI
- 10.1186/s12887-021-02771-4
- Published
- 2021-06-28
- Container
- BMC Pediatrics
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s12887-021-02771-4,
title = {Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report},
author = {Zhanhui Du and Gang Luo and Kuiliang Wang and Zhen Bing and Silin Pan},
year = {2021},
journal = {BMC Pediatrics},
doi = {10.1186/s12887-021-02771-4},
url = {https://doi.org/10.1186/s12887-021-02771-4}
}RIS
TY - JOUR TI - Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report AU - Zhanhui Du AU - Gang Luo AU - Kuiliang Wang AU - Zhen Bing AU - Silin Pan PY - 2021 JO - BMC Pediatrics DO - 10.1186/s12887-021-02771-4 UR - https://doi.org/10.1186/s12887-021-02771-4 ER -
APA
Du, Z., Luo, G., Wang, K., Bing, Z., & Pan, S. (2021). Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report. BMC Pediatrics. https://doi.org/10.1186/s12887-021-02771-4
Source records
- crossref · retrieved 2026-09-25T20:30:59.294Z