[1] Di LV, Licchetta L, Pippucci T, et al. Phenotype variability of GLUT1 deficiency syndrome:Description of a case series with novel SLC2A1 gene mutations[J]. Epilepsy Behav, 2018, 79:169-173. [2] 姬辛娜,徐翠娟,高志杰,等.葡萄糖转运子1缺陷综合征运动障碍特点和诊疗分析[J].中国当代儿科杂志,2018,20(3):209-213. [3] Benarroch EE. Brain glucose transporters:implications for neurologic disease[J].Neurology, 2014, 82(15):1374-1379. [4] Szczepanik E, Terczyńska I, Kruk M, et al. Glucose transporter type 1 deficiency due to SLC2A1 gene mutations-a rare but treatable cause of metabolic epilepsy and extrapyramidal movement disorder; own experience and literature review[J]. Dev Period Med, 2015, 19(4):454-463