The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome

Overview of attention for article published in Epilepsia, November 2015

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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy and the estimated frequency of GLUT1 https://t.co/5sazXhSSBe

SLC2A1 in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1-DS https://t.co/9hJOSAcbRY #Neurology

The role of SLC2A1 mutation in myoclonic astatic epilepsy and absence epilepsy and the frequency of GLUT1 deficiency https://t.co/IF3ny9sKoi

The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the frequency of GLUT1syndrome https://t.co/QbyA0pvgka

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