Background: Epilepsy in childhood is a common and diverse neurological disorder. We conducted a genetic and phenotype analysis of a Chinese cohort of infants and children with epilepsy. Methods: We co
Coexpression analysis indicates that the heterozygous mutations of KCNC1, CAPN3, NEFH and APOB were closely related to the clinical phenotypes of the patient, and the clinical phenotypic heterogeneity
