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Medicin og biovidenskab

Mutation
Exome
Rolandic Epilepsy
Electroencephalography
Genetic Association Studies
Microcephaly
Absence Epilepsy
Febrile Seizures
Malformations of Cortical Development
Genetic Heterogeneity
Movement Disorders
Reflex Epilepsy
Proteins
Rett Syndrome
Neuroimaging
Mosaicism
Comparative Genomic Hybridization
Glycosylphosphatidylinositols
Muscle Hypotonia
GABA-A Receptors
Haploinsufficiency
Adaptor Protein Complex 4
Parents
Missense Mutation
Genome-Wide Association Study
Case-Control Studies
Juvenile Myoclonic Epilepsy
Language Development Disorders
Valine-tRNA Ligase
Zebrafish
Population
Dynamin I
Diazepam Binding Inhibitor
Methyl-CpG-Binding Protein 2
Congenital Disorders of Glycosylation
Hereditary Spastic Paraplegia
Genetic Counseling