Angelman syndrome: clinical findings and follow-up data of 14 patients

The diagnosis of Angelman syndrome (AS) is based on the clinical features, behavior, EEG findings, and genetic abnormalities. The physical, clinical and behavioral aspects appear to attributable to localized central nervous system (CNS) dysfunction of the ubiquitin ligase gene, UBE3A, located...

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Bibliographic Details
Main Authors: Bülent Kara, Birsen Karaman, Meral Ozmen, Rasim Ozgür Rosti, Mine Calişkan, Hülya Kayserili, Seher Başaran
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 2008-04-01
Series:The Turkish Journal of Pediatrics
Online Access:https://turkjpediatr.org/article/view/2399
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