Pediatric Neurology Briefs (Oct 2011)

Glucose Transporter 1 Deficiency and Myoclonic Astatic Epilepsy

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-25-10-6
Journal volume & issue
Vol. 25, no. 10
pp. 77 – 77

Abstract

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Researchers at University of Melbourne, Australia; University of Florence, Italy; and University of Antwerp, Belgium performed genetic analysis on 84 unrelated probands with myoclonic-astatic epilepsy (MAE).

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