Clinical Variability of GLUT1DS

Investigators from Pavia, Rho, Brescia and Milan, Italy, studied 22 patients diagnosed with GLUT1 deficiency syndrome (GLUT1DS) to document clinical or genetic differences between patients with familial SLC2A1 gene mutations (n=11) and those with sporadic mutations (n=11).

Bibliographic Details
Main Authors: Melnikova, Anastasia Martinez-Esteve, Korff, Christian M.
Format: Online
Language:English
Published: Pediatric Neurology Briefs Publishers 2015
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747289/