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| Pediatric Neurology Briefs: Volume 26, Issue 02 |
POLG Novel Mutation with Alpers Syndrome Open Access (recommended)
Descriptions
- Resource type(s)
- Article
- Keyword
- POLG Mutations
VPA-Induced Fatal Liver Failure
Alpers Syndrome
- Rights
- Attribution 4.0 International
- Creator
-
Millichap, J. Gordon
- Abstract
-
Researchers at University Hospital, Berne, Switzerland describe the molecular genetic analysis of POLG in a 3.5 years old boy with VPA-induced fatal liver failure and encephalopathy (Alpers-Huttenlocher syndrome, AHS).
- Publisher
-
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
- Date Created
-
2012
- Original Identifier
- PNB-2012-26-2-5
- Language
- English
- Subject: MESH
-
Child
Neurology
Infant
Nervous System Diseases
Brain Diseases
Neurosurgery
Pediatrics
Child Development
- DOI
-
10.15844/pedneurbriefs-26-2-5
File Details
- File Properties
-
Mime type: application/pdf
File size: 105.7 kB