A de novo SCN8A heterozygous mutation in a child with epileptic encephalopathy: a case report
- DOI
- 10.1186/s12887-019-1796-9
- Published
- 2019-11-01
- 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/s12887-019-1796-9,
title = {A de novo SCN8A heterozygous mutation in a child with epileptic encephalopathy: a case report},
author = {Kao-Min Lin and Geng Su and Fengpeng Wang and Xiaobin Zhang and Yuanqing Wang and Jun Ren and Xin Wang and Yi Yao and Ying Zhou},
year = {2019},
journal = {BMC Pediatrics},
doi = {10.1186/s12887-019-1796-9},
url = {https://doi.org/10.1186/s12887-019-1796-9}
}RIS
TY - JOUR TI - A de novo SCN8A heterozygous mutation in a child with epileptic encephalopathy: a case report AU - Kao-Min Lin AU - Geng Su AU - Fengpeng Wang AU - Xiaobin Zhang AU - Yuanqing Wang AU - Jun Ren AU - Xin Wang AU - Yi Yao AU - Ying Zhou PY - 2019 JO - BMC Pediatrics DO - 10.1186/s12887-019-1796-9 UR - https://doi.org/10.1186/s12887-019-1796-9 ER -
APA
Lin, K., Su, G., Wang, F., Zhang, X., Wang, Y., Ren, J., Wang, X., Yao, Y., & Zhou, Y. (2019). A de novo SCN8A heterozygous mutation in a child with epileptic encephalopathy: a case report. BMC Pediatrics. https://doi.org/10.1186/s12887-019-1796-9
Source records
- crossref · retrieved 2026-09-26T04:53:53.543Z