De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin
Sarah E Heron, Ingrid E Scheffer, Xenia Iona, Sameer M Zuberi, Rachael Birch, Jacinta M McMahon, Carla M Bruce, Samuel F Berkovic, John C Mulley
Journal of Medical Genetics | B M J PUBLISHING GROUP | Published : 2010
We thank the patients and their parents for participation in this study. Patients were referred by the Infantile Epileptic Encephalopathy Referral Consortium. This work was supported by the National Health and Medical Research Council of Australia.National Health and Medical Research Council of Australia, GPO Box 1421, Canberra ACT 2601, Australia.