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Publications by Deb K. Pal
A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy
American Journal of Human Genetics
Genetics
Clinical Spectrum of STX1B-related Epileptic Disorders
Neurology
Neurology
A Neurocognitive Endophenotype Associated With Rolandic Epilepsy
Epilepsia
Neurology
Imaging and Genetics of Language and Cognition in Pediatric Epilepsy
Epilepsy and Behavior
Neurology
Behavioral Neuroscience
BRD2 (RING3) Is a Probable Major Susceptibility Gene for Common Juvenile Myoclonic Epilepsy
American Journal of Human Genetics
Genetics
An Autosomal Dominant Genetically Heterogeneous Variant of Rolandic Epilepsy and Speech Disorder
Epilepsia
Neurology
Autosomal Dominant Inheritance of Centrotemporal Sharp Waves in Rolandic Epilepsy Families
Epilepsia
Neurology