Jaafar, A., Alsiddiq, F. and Ling, K. H. (2018) “Pathogenic mutations in ARX, CDKL5 and STXBP1 genes are not associated with the early-onset epileptic encephalopathy in Malaysian pediatric patients: A pilot study”, Neuroscience Research Notes, 1(3), pp. 5-17. doi: 10.31117/neuroscirn.v1i3.16.