Comments on: SCN1A Genetic Test for Dravet Syndrome (Severe Myoclonic Epilepsy of Infancy and its Clinical Subtypes) for use in the Diagnosis, Prognosis, Treatment and Management of Dravet Syndrome

Comments on: SCN1A Genetic Test for Dravet Syndrome (Severe Myoclonic Epilepsy of Infancy and its Clinical Subtypes) for use in the Diagnosis, Prognosis, Treatment and Management of Dravet Syndrome https://currents.plos.org/genomictests/article/scn1a-genetic-test-for-dravet-syndrome-severe-myoclonic-epilepsy-of-infancy-and-its-clinical-subtypes/ Fri, 11 Aug 2017 16:36:40 +0000 hourly 1 https://wordpress.org/?v=4.5.3