Phenotype variability of GLUT1 deficiency syndrome: Description of a case series with novel SLC2A1 gene mutations.

Phenotype variability of GLUT1 deficiency syndrome: Description of a case series with novel SLC2A1 gene mutations.
Epilepsy Behav. 2018 Jan 03;79:169-173
Authors: Di Vito L, Licchetta L, Pippucci T, Baldassari S, Stipa C, Mostacci B, Alvisi L, Tinuper P, Bisulli F
PMID: 29306089 [PubMed - as supplied by publisher]

Source: Epilepsy and Behaviour - January 3, 2018 Category: Neurology Authors: Di Vito L, Licchetta L, Pippucci T, Baldassari S, Stipa C, Mostacci B, Alvisi L, Tinuper P, Bisulli F Tags: Epilepsy Behav Source Type: research