Seizure Characterization and Electroencephalographic Features in Glut-1 Deficiency Syndrome
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1528-1157.2003.05302.x/fullpdf
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2. Glucose transport protein deficiency: an emerging syndrome with therapeutic implications.;De Vivo;Int Pediatr,1995
3. Autosomal dominant Glut-1 deficiency syndrome and familial epilepsy.;Brockmann;Ann Neurol,2001
4. Erythrocyte 3-O-methyl-D-glucose uptake assay for diagnosis of glucose-transporter-protein syndrome.;Klepper;J Clin Lab Anal,1999
5. Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3-p35.;Shows;Diabetes,1987
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