Allelic Variations of Glut1 Deficiency Syndrome: The Chinese Experience
Liu Y, Bao XH, Wang D, Fu N, Zhang XY, Cao GN, Song FY, Wang S, Zhang YH, QinJ, Yang H, Engelstad K, De Vivo DC, Wu XR, Pediatr Neurol, 1/1/2012T295M associated glut-1 deficiency syndrome with normal erythrocyte 3-OMG uptake
Fuji T, Morimoto M, Yoshioka H, Ho YY, Law PY, Wang D, De Vivo DC, Brain Dev, 1/1/2011Uncovering Microdeletions in Patients with Severe Glut-1 Deficiency Syndrome Using SNP Oligonucleotide Microarray Analysis
Levy B, Wang D, Ullner PM, Engelstad K, Yang H, Nahum O, Chung WK, De Vivo DC, Molecular Genetics and Metabolism, 1/1/2010
