Clinical analysis of CHD2 gene mutations in pediatric patients with epilepsy
Author:
Affiliation:
1. Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China
Funder
National Natural Science Foundation of China
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ped4.12321
Reference28 articles.
1. CHD2-Related CNS Pathologies
2. CHD2 ‐related epilepsy: novel mutations and new phenotypes
3. CHD2variants are a risk factor for photosensitivity in epilepsy
4. Analysis of the Electrical Response of the Human Cortex to Photic Stimulation
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1. Clinical analysis of five CHD2 gene mutations in Chinese children with epilepsy;Seizure: European Journal of Epilepsy;2024-10
2. Expanding the Mutational Landscape and Clinical Phenotype of CHD2-Related Encephalopathy;Neurology Genetics;2024-08
3. Low‐grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis‐like syndrome;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2024-02-22
4. Genotype Mutations and Phenotypes of 30 Cases with Epilepsy Related to Fever Sensitivity in Children;2024
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