Recessive mutations in<i>SLC13A5</i>result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasiaKatia Hardies(University of Antwerp), Bobby P. C. Koeleman(Utrecht University)BrainSeptember 17, 201510.1093/brain/awv263Cited by 111SaveCiteExport RISWatch citationsRelated PapersBi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy|Brain|2020|32