Glucose Transporter 1 Deficiency and Myoclonic Astatic Epilepsy
Abstract
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).
DOI: https://doi.org/10.15844/pedneurbriefs-25-10-6 | Journal eISSN: 2166-6482
Language: English
Page range: 77 - 77
Published on: Oct 1, 2011
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2011 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.