Publication
Title
De novo SCN1A mutations ara a major cause of severe myoclonic epilepsy of infancy
Author
Language
English
Source (journal)
Human mutation. - New York, N.Y.
Publication
New York, N.Y. : 2003
ISSN
1059-7794
Volume/pages
21(2003), p. 615-621
ISI
000183395500009
Full text (Publisher's DOI)
UAntwerpen
Faculty/Department
Research group
Publication type
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 08.10.2008
Last edited 15.06.2017
To cite this reference