Journal article

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

Grants

Funding Acknowledgements

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.