SCN8A-related disorders are a group of variable conditions caused by pathogenic variations in SCN8A. Online Mendelian Inheritance in Man (OMIM) terms them as developmental and epileptic encephalopathy 13, benign ...
Authors:
Malavika Hebbar, Nawaf Al-Taweel, Inderpal Gill, Cyrus Boelman, Richard A. Dean, Samuel J. Goodchild, Janette Mezeyova, Noah Gregory Shuart, J. P. Johnson Jr., James Lee, Aspasia Michoulas, Linda L. Huh, Linlea Armstrong, Mary B. Connolly and Michelle K. Demos
Citation:
BMC Neurology
2024
24:31
Content type: Case Report
Published on: 17 January 2024