Sturge-Weber Syndrome Linked to GNAQ Mutation

Sturge-Weber Syndrome Linked to GNAQ Mutation

Investigators from Johns Hopkins School of Medicine, the Hugo W Moser Research Institute at Kennedy Krieger, Baltimore; Duke University; and Medical College of Wisconsin, Milwaukee, performed whole-genome sequencing of DNA from paired samples of tissue from 3 persons with the Sturge-Weber syndrome (...

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Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 2013-07-01
Series:Pediatric Neurology Briefs
Subjects:
sturge-weber syndrome
vascular endothelial cells
gnaq mutation
Online Access:https://www.pediatricneurologybriefs.com/articles/404
Description
Summary:Investigators from Johns Hopkins School of Medicine, the Hugo W Moser Research Institute at Kennedy Krieger, Baltimore; Duke University; and Medical College of Wisconsin, Milwaukee, performed whole-genome sequencing of DNA from paired samples of tissue from 3 persons with the Sturge-Weber syndrome (SWS).
ISSN:1043-3155
2166-6482

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