Associated Papers
Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation.
Traynelis J et al.
Genome Research, 2017
28864458 (PubMed )
Supplement: supp_gr.226589.117_Supplemental_Data_S1.xlsx › Data_S1
Sporadic and familial glut1ds Italian patients: A wide clinical variability.
De Giorgis V et al.
Seizure, 2015
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.
Klepper J et al.
Febs Letters, 2001
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