المؤلفون: Wen‐Jun Zhang, Tao Su, Wei-Wen Deng, Min‐Zhi Zhuang, Xiao-Rong Liu, Ting-Ting Ye, Meng Xu, Xing-Wang Song, Jie Wang, Long‐Shan Xie, Yong-Hong Yi, Na He, Qian‐Yi Wu, Bing-Mei Li, Wei-Ping Liao, Shao‐Ping Huang, Yi-Wu Shi, Xuan Guo

المصدر: CNS Neuroscience & Therapeutics

مصطلحات موضوعية: 0301 basic medicine, Male, Adolescent, Genotype, sinus arrhythmia, Mutation, Missense, Chromodomain, Cohort Studies, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Physiology (medical), Exome Sequencing, Medicine, Missense mutation, Humans, Pharmacology (medical), Arrhythmia, Sinus, Child, Gene, Sinus (anatomy), CHD4 gene, Pharmacology, Genetics, business.industry, Genetic Variation, Electroencephalography, Original Articles, Middle Aged, medicine.disease, Phenotype, Psychiatry and Mental health, 030104 developmental biology, medicine.anatomical_structure, Cohort, childhood idiopathic epilepsy, Mutation, Original Article, Female, CHD4, business, 030217 neurology & neurosurgery, Mi-2 Nucleosome Remodeling and Deacetylase Complex

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01e9aef620a0f65c89a70a3b14c3818f
http://europepmc.org/articles/PMC8446219