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Publications by Yvonne G. Weber
A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy
American Journal of Human Genetics
Genetics
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
American Journal of Human Genetics
Genetics
Clinical Spectrum of STX1B-related Epileptic Disorders
Neurology
Neurology
Development of a Rapid Functional Assay That Predicts GLUT1 Disease Severity
Neurology: Genetics
Neurology
Genetics
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