Dimitri M Kullmann. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Epilepsy/classificationEpilepsy/etiologyEpilepsy/geneticsGenetic Predisposition to Disease/geneticsHumansInheritance PatternsIon Channel Gating/geneticsMutation
Year: 2002 PMID: 12536158 PMCID: PMC1765606 DOI: 10.1136/jnnp.73.suppl_2.ii32
Source DB: PubMed Journal: J Neurol Neurosurg Psychiatry ISSN: 0022-3050 Impact factor: 10.154