Genotype-phenotype correlations in SCN8A-related epilepsy: a cohort study of Chinese children in southern China
Brain
.
2022 May 24;145(4):e24-e27.
doi: 10.1093/brain/awac038.
Authors
Bing-Wei Peng
1
,
Yang Tian
1
,
Li Chen
2
,
Li-Fen Duan
3
,
Xiu-Ying Wang
1
,
Hai-Xia Zhu
1
,
Kai-Li Shi
1
,
Ke-Lu Zheng
1
,
Hui-Ling Shen
1
,
Wei Liang
1
,
Xiao-Jing Li
1
,
Wen-Xiong Chen
1
Affiliations
1
Department of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
2
Epilepsy Treatment Center, Shenzhen Children's Hospital, Shenzhen, Guangdong, China.
3
Division of Neurology, The Kunming Children's Hospital, Kunming, Yunnan, China.
PMID:
35230384
PMCID:
PMC9129090
DOI:
10.1093/brain/awac038
No abstract available
Publication types
Editorial
Comment
MeSH terms
China / epidemiology
Cohort Studies
Epilepsy* / genetics
Genetic Association Studies
Humans
NAV1.6 Voltage-Gated Sodium Channel / genetics
Substances
NAV1.6 Voltage-Gated Sodium Channel
SCN8A protein, human