Skip to Content

Coronavirus information for Feinberg.

Download the full-sized PDF of PI3K/AKT Pathway and Brain Malformations
Download the file

Actions

Download Analytics Citations

Export to: EndNote

Collections

This file is in the following collections:

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