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
Log likelihood and posterior probability of the phenotypes conditional on the pedigree, founder genotypes and model of inheritance. Z is a sex chromosome. The prior probability of each model is unifor
This file (947 rows x 3 columns) gives, for the PPS653 population (Jean Pied de Port 3 , W-SWF) the pedigree of observed full-sib ears. The format is that used in ASReml.
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
