No abstract available
Keywords:
Epilepsy; Glucose transporter type I deficiency syndrome; Nonepileptic paroxysmal phenomena; SLC2A1 mutation.
MeSH terms
-
Adult
-
Carbohydrate Metabolism, Inborn Errors / genetics*
-
Epilepsy, Generalized / complications*
-
Epilepsy, Generalized / genetics*
-
Female
-
Genetic Variation / genetics*
-
Glucose Transporter Type 1 / genetics*
-
Humans
-
Male
-
Monosaccharide Transport Proteins / deficiency*
-
Monosaccharide Transport Proteins / genetics
-
Mutation
-
Phenotype
-
Seizures / etiology*
Substances
-
Glucose Transporter Type 1
-
Monosaccharide Transport Proteins
-
SLC2A1 protein, human
Supplementary concepts
-
Glut1 Deficiency Syndrome