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Pediatric Neurology Briefs: Volume 16, Issue 01

Autosomal Dominant Epilepsy Syndrome Linked to 2p11 Open Access (recommended)

Descriptions

Resource type(s)
Article
Keyword
Cortical Origin
Valproate
Contralateral Rolandic Area
Rights
Attribution 4.0 International

Creator
Millichap, J. Gordon
Abstract
A newly recognized autosomal dominant epilepsy syndrome with linkage to chromosome 2p11.1-q12.2 is described in an Italian pedigree of 8 patients reported from the Neurosciences Unit, Institute of Child Health and Great Ormond Street Hospital for Children, London, UK.
Publisher
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
Date Created
2002
Original Identifier
PNB-16-03-b
Language
English
Subject: MESH
Neurology
Child Development
Nervous System Diseases
Neurosurgery
Brain Diseases
Child
Pediatrics
Infant
DOI
10.15844/pedneurbriefs-16-1-4

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