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