TY  - GEN
AU  - Di Vito,Lidia
AU  - Licchetta,Laura
AU  - Pippucci,Tommaso
AU  - Baldassari,Sara
AU  - Stipa,Carlotta
AU  - Mostacci,Barbara
AU  - Alvisi,Lara
AU  - Tinuper,Paolo
AU  - Bisulli,Francesca
TI  - Phenotype variability of GLUT1 deficiency syndrome: Description of a case series with novel SLC2A1 gene mutations
SN  - 1525-5069
PY  - 2018///1221
KW  - Adult
KW  - Carbohydrate Metabolism, Inborn Errors
KW  - genetics
KW  - Epilepsy, Generalized
KW  - complications
KW  - Female
KW  - Genetic Variation
KW  - Glucose Transporter Type 1
KW  - Humans
KW  - Male
KW  - Monosaccharide Transport Proteins
KW  - deficiency
KW  - Mutation
KW  - Phenotype
KW  - Seizures
KW  - etiology
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1016/j.yebeh.2017.12.012
ER  -