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Phenotype variability of GLUT1 deficiency syndrome: Description of a case series with novel SLC2A1 gene mutations.

Epilepsy & behavior : E&B - 1 Feb 2018

Di Vito Lidia, Licchetta Laura, Pippucci Tommaso, Baldassari Sara, Stipa Carlotta, Mostacci Barbara, Alvisi Lara, Tinuper Paolo, Bisulli Francesca

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Share to Carbohydrate Metabolism, Inborn Errors
Share to Epilepsy, Generalized
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucose Transporter Type 1

Share to Monosaccharide Transport Proteins

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Identifiers

PMID: 29306089
DOI: 10.1016/j.yebeh.2017.12.012

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