Genetics of Severe Myoclonic Epilepsy of Infancy
Abstract
The role of SCN1A gene mutations in the etiology of severe myoclonic epilepsy of infancy (SMEI) was investigated in 93 patients followed at the Hopital Saint Vincent de Paul, Paris, and other centers in France and Italy.
DOI: https://doi.org/10.15844/pedneurbriefs-17-7-3 | Journal eISSN: 2166-6482
Language: English
Page range: 51 - 51
Published on: Jul 1, 2003
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2003 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.