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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
2019English

Clinical Spectrum of STX1B-related Epileptic Disorders

Neurology
Neurology
2019English

A Neurocognitive Endophenotype Associated With Rolandic Epilepsy

Epilepsia
Neurology
2012English

Imaging and Genetics of Language and Cognition in Pediatric Epilepsy

Epilepsy and Behavior
NeurologyBehavioral Neuroscience
2013English

BRD2 (RING3) Is a Probable Major Susceptibility Gene for Common Juvenile Myoclonic Epilepsy

American Journal of Human Genetics
Genetics
2003English

An Autosomal Dominant Genetically Heterogeneous Variant of Rolandic Epilepsy and Speech Disorder

Epilepsia
Neurology
2008English

Autosomal Dominant Inheritance of Centrotemporal Sharp Waves in Rolandic Epilepsy Families

Epilepsia
Neurology
2007English

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