Genetic Heterogeneity in Familial Nocturnal Frontal Lobe Epilepsy
Ortrud K. Steinlein
Potassium Channel Genes and Benign Familial Neonatal Epilepsy
Snezana Maljevic and Holger Lerche
Mutant GABAA Receptor Subunits in Genetic (Idiopathic) Epilepsy
Shinichi Hirose
The Role of Calcium Channel Mutations in Human Epilepsy
Antonio Gambardella and Angelo Labate
Mechanisms Underlying Epilepsies Associated with Sodium Channel Mutations
Ortrud K. Steinlein
The Progressive Myoclonus Epilepsies
Berge A. Minassian
Genetics Advances in Autosomal Dominant Focal Epilepsies: Focus on DEPDC5
Stephanie Baulac
PRRT2: A Major Cause of Infantile Epilepsy and other Paroxysmal Disorders of Childhood
Carlo Nobile and Pasquale Striano
LGI1: From Zebrafish to Human Epilepsy
John K. Cowell
Morphogenesis and Timing of Genetically-Programmed Brain Malformations in Relation to Epilepsy
Harvey B. Sarnat and Laura Flores-Sarnat
Remind Me Again What Disease We are Studying? A Population Genetics, Genetic Analysis, and Real Data Perspective on Why Progress on Identifying Genetic Influences on Common Epilepsies has Been So Slow
David A. Greenberg and William L. Stewart
Monogenic Models of Absence Epilepsy: Windows into the Complex Balance between Inhibition and Excitation in Thalamocortical Microcircuits
Atul Maheshwari and Jeffrey L. Noebels
New Technologies in Molecular Genetics: The Impact on Epilepsy Research
Ingo Helbig
Epigenetic Mechanisms in Epilepsy
Katja Kobow and Ingmar Bluemcke
