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

Publisher： John Wiley & Sons Inc

E-ISSN： 1528-1167|56|12|e203-e208

ISSN： 0013-9580

Source： EPILEPSIA, Vol.56, Iss.12, 2015-12, pp. : e203-e208

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