Madaan, Priyanka
Jeavons syndrome in a family with GLUT1-deficiency syndrome. [electronic resource]
- Seizure 10 2019
- 158-160 p. digital
Publication Type: Case Reports; Journal Article
1532-2688
10.1016/j.seizure.2019.07.011 doi
Carbohydrate Metabolism, Inborn Errors--genetics
Child
Drug Resistant Epilepsy--genetics
Epileptic Syndromes--genetics
Glucose Transporter Type 1--deficiency
Humans
Male
Monosaccharide Transport Proteins--deficiency
Mutation, Missense
Myoclonus--genetics