We are pleased to share with our families a presentation titled, “Understand Genetic Research and Alternating Hemiplegia of Childhood.” The presentation was created to help answer questions about the process of genetic research and introduce families to the ATP1A3 gene mutation. We hope you will share this presentation with your friends and family as one more tool to help understand AHC.
For more information please refer to Dr Kathryn Swoboda’s Pediatric Motor Disorder Research Program website http://medicine.utah.edu/neurology/research/swoboda/research/index.htm
For specific Genetics questions please contact Tara Newcomb at the University of Utah <email@example.com>Presentation (PDF format)
Alternating Hemiplegia of Childhood Foundation
2000 Town Center Suite 1900
Southfield, MI 48075