High prevalence of short-chain acyl-CoA dehydrogenase deficiency in the Netherlands, but no association with epilepsy of unknown origin in childhood. [electronic resource]
Producer: 20110908Description: 13-7 p. digitalISSN:- 1439-1899
- Acyl-CoA Dehydrogenase -- deficiency
- Adolescent
- Butyryl-CoA Dehydrogenase -- genetics
- Child
- Child, Preschool
- DNA Mutational Analysis
- Epilepsy -- epidemiology
- Female
- Humans
- Incidence
- Infant
- Infant, Newborn
- Lipid Metabolism, Inborn Errors -- diagnosis
- Male
- Mutation -- genetics
- Netherlands -- epidemiology
- Pediatrics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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