| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3037756 | Brain and Development | 2011 | 4 Pages |
Abstract
Glucose transporter type 1 deficiency syndrome (GLUT1DS) is increasingly recognized as a cause of various neurological disorders but a high index of suspicion is important to make the diagnosis. We report two Chinese patients with GLUT1DS, one of which had a novel mutation in the SLC2A1 gene.
Keywords
Related Topics
Life Sciences
Neuroscience
Developmental Neuroscience
Authors
Eva Lai-wah Fung, Yuan Yuan Ho, Joannie Hui, Jack Ho Wong, Tzi-Bun Ng, Nga-Yin Fion Fong, Joerg Klepper, Kwok-Wing Stephen Tsui,