Indications for Genetic Testing for Dravet Syndrome

Researchers at the Cincinnati Children's Medical Center, OH investigated the predictive value of features of Dravet syndrome, as defined by the International League Against Epilepsy, as criteria for a positive SCN1A gene mutation in a cohort of consecutively tested children.

Saved in:
Bibliographic Details
Main Author: J Gordon Millichap (Author)
Format: Book
Published: Pediatric Neurology Briefs Publishers, 2011-11-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available