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Pediatric Neurology Briefs: Volume 15, Issue 10

Glut-1 Deficiency Syndrome and Familial Epilepsy Open Access (recommended)

Descriptions

Resource type(s)
Article
Keyword
Mild Ataxia-Dystonia
Antiepileptic Drugs
Deficiency Syndrome
Rights
Attribution 4.0 International

Creator
Millichap, J. Gordon
Abstract
A family with autosomal dominant Glut-1 deficiency syndrome (DS) affecting 5 members over 3 generations is reported from the University of Goettingen, Germany; and Columbia University, New York.
Publisher
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
Date Created
2001
Original Identifier
PNB-15-74
Language
English
Subject: MESH
Infant
Nervous System Diseases
Neurosurgery
Child Development
Neurology
Brain Diseases
Child
Pediatrics
DOI
10.15844/pedneurbriefs-15-10-2

File Details

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Mime type: application/pdf
File size: 2960.1 kB