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Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene

Compound Heterozygous MutationMendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseMolecular BiologyMolecular Genetics4-Aminobutyrate AminotransferaseAbnormal DevelopmentStereotypic Movement DisorderMedicineHypersomnolence-hyperkinetic Movement DisorderMonogenic Disorders