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| Pediatric Neurology Briefs: Volume 26, Issue 11 |
Paroxysmal Kinesigenic Dyskinesia and Infantile Convulsions Open Access (recommended)
Descriptions
- Resource type(s)
- Article
- Keyword
- Benign Familial Infantile Convulsions
Infantile Convulsion and Choreoathetosis
Heterozygous Mutations
- Rights
- Attribution 4.0 International
- Creator
-
Millichap, J. Gordon
- Abstract
-
A team of twelve geneticists and neurologists from centers in the Netherlands studied the phenotypes and penetrance of paroxysmal kinesigenic dyskinesia (PKD), infantile convulsion and choreoathetosis (ICCA) syndrome, and benign familial infantile convulsions (BFIC), caused by PRRT2 mutations.
- Publisher
-
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
- Date Created
-
2012
- Original Identifier
- PNB-2012-26-11-6
- Language
- English
- Subject: MESH
-
Movement Disorders
Child Development
Child
Nervous System Diseases
Neurosurgery
Neurology
Pediatrics
Infant
Brain Diseases
- DOI
-
10.15844/pedneurbriefs-26-11-6
File Details
- File Properties
-
Mime type: application/pdf
File size: 97.1 kB