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| Pediatric Neurology Briefs: Volume 29, Issue 07 |
PI3K/AKT Pathway and Brain Malformations Open Access (recommended)
Descriptions
- Resource type(s)
- Article
- Keyword
- Megalencephaly
Cortical dysplasia
PI3K/AKT mutations
- Rights
- Attribution 4.0 International
- Creator
-
Rice, Gavin B.
Wadhwani, Nitin R.
- Abstract
-
Investigators from Seattle Children's Research Institute, University of Washington, and collaborating institutions sought to evaluate 10 genes in the PI3K/AKT pathway as it relates epileptogenic brain malformations in patients with megalencephaly, hemimegalencephaly, and focal cortical dysplasia.
- Publisher
-
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
- Date Created
-
2015
- Original Identifier
- PNB-29-52
- Language
- English
- Subject: MESH
-
Infant
Brain Diseases
Pediatrics
Neurology
Child Development
Nervous System Diseases
Child
Neurosurgery
- DOI
-
10.15844/pedneurbriefs-29-7-3
File Details
- File Properties
-
Mime type: application/pdf
File size: 135.5 kB