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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

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Mime type: application/pdf
File size: 97.1 kB