A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome

Authors

Nanda A. Singh, University of Utah
Chris Pappas, University of Utah
E. Jill Dahle, University of Utah
Lieve R. F. Claes, University of Antwerp
Timothy H. Pruess, University of Utah
Peter De Jonghe, University of Antwerp
Joel Thompson, University of Utah
Missy Dixon, University of Utah
Christina Gurnett, Washington University School of Medicine in St. Louis
Andy Peiffer, University of Utah
H. Steve White, University of Utah
Francis Filloux, University of Utah
Mark F. Leppert, University of Utah

Journal

PLoS Genetics

Publication Date

2009

Volume

5

Issue

9

Inclusive Pages

e1000649

Document Type

Open Access Publication

DOI

10.1371/journal.pgen.1000649

Rights and Permissions

Singh NA, Pappas C, Dahle EJ, Claes LRF, Pruess TH, et al. (2009) A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome. PLoS Genet 5(9): e1000649. doi:10.1371/journal.pgen.1000649

Recommended Citation

Singh, Nanda A.; Pappas, Chris; Dahle, E. Jill; Claes, Lieve R. F.; Pruess, Timothy H.; De Jonghe, Peter; Thompson, Joel; Dixon, Missy; Gurnett, Christina; Peiffer, Andy; White, H. Steve; Filloux, Francis; and Leppert, Mark F., "A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome." PLoS Genetics. 5, 9. e1000649. (2009).
https://digitalcommons.wustl.edu/open_access_pubs/1004