Dravet syndrome (DS) is a severe childhood-onset epileptic encephalopathy caused by SCN1A mutations.[1] However, it was recently reported that this syndrome can sometimes also be caused by STXBP1 mutations.[2]
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Dravet syndrome (DS) is a severe childhood-onset epileptic encephalopathy caused by SCN1A mutations.[1] However, it was recently reported that this syndrome can sometimes also be caused by STXBP1 mutations.[2]