Published 2010
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Early-Onset Epileptic Encephalopathies with STXBPl Mutations
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Abstract
Researchers at the Department of Molecular Genetics, University of Antwerp, and other centers in Belgium, The Netherlands, and Melbourne, Australia, analyzed the clinical phenotypes associated with STXBPl mutations in a cohort of 106 patients with unexplained early-onset epileptic encephalopathies.Files
PNB-24-89.pdf
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- PNB-24-89
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2010When the item was originally created.