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Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects.
- Source :
- Seizure; Jan2012, Vol. 21 Issue 1, p17-20, 4p
- Publication Year :
- 2012
Details
- Language :
- English
- ISSN :
- 10591311
- Volume :
- 21
- Issue :
- 1
- Database :
- Supplemental Index
- Journal :
- Seizure
- Publication Type :
- Academic Journal
- Accession number :
- 104619146