Analysis of clinical phenotype and gene variation characteristics of potassium channel gene variation in infants with epileptic encephalopathy
Objective To analyze and summarize the clinical and genetic characteristics of potassium channel gene variation in infant epileptic encephalopathy (EE). Methods and Results A total of 11 infants with EE associated with potassium channel gene variation admitted to Hu'nan Children's Hospital...
Main Authors: | XU Rong, NING Ze⁃shu, KANG Qing⁃yun, CHEN Bo, LIAO Hong⁃mei, YANG Li⁃ming, WU Li⁃wen |
---|---|
Format: | Article |
Language: | English |
Published: |
Tianjin Huanhu Hospital
2023-03-01
|
Series: | Chinese Journal of Contemporary Neurology and Neurosurgery |
Subjects: | |
Online Access: | http://www.cjcnn.org/index.php/cjcnn/article/view/2646 |
Similar Items
-
Potassium channels and human epileptic phenotypes: an updated overview
by: Chiara eVilla, et al.
Published: (2016-03-01) -
The study of sodium and potassium channel gene single-nucleotide variation significance in non-mechanical forms of epilepsy
by: Ozada Khamdiyeva, et al.
Published: (2021-01-01) -
Clinical phenotype, gene mutation and application of targeted next generation sequencing in patients with early-onset epileptic encephalopathy
by: Xiao-jun LIU, et al.
Published: (2018-06-01) -
The Impact of Potassium Channel Gene Polymorphisms on Antiepileptic Drug Responsiveness in Arab Patients with Epilepsy
by: Laith N. AL-Eitan, et al.
Published: (2018-11-01) -
Recurrent and non-recurrent mutations of SCN8A in epileptic encephalopathy
by: Jacy L Wagnon, et al.
Published: (2015-05-01)