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 <em>SLC2A1</em> gene mutations (n=11) and those with sporadic mutations (n=11).
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2015-02-01
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| Series: | Pediatric Neurology Briefs |
| Subjects: | |
| Online Access: | https://www.pediatricneurologybriefs.com/articles/39 |