ATP1A3 mutations can disrupt a child’s ability to move, speak, and grow, starting as early as infancy. This rare genetic disorder reveals how one gene can reshape a life. Read the full story: https://bit.ly/3Pq5u9E #ATP1A3  #MovementDisorders #ChildNeurology  #PediatricHealth  #MedicalResearch

ATP1A3 mutations can disrupt a child’s ability to move, speak, and grow, starting as early as infancy. This rare genetic disorder reveals how one gene can reshape a life. Read the full story: https://bit.ly/3Pq5u9E #ATP1A3  #MovementDisorders #ChildNeurology  #PediatricHealth  #MedicalResearch

Novel mouse model of alternating hemiplegia of childhood exhibits prominent motor and seizure phenotypes Pathogenic variants in ATP1A3 encoding the neuronal Na/K-ATPase cause a spectrum of neurodevelopmental disorders including alternating hemiplegia of c…

Thankful to peer reviewers who constructively reviewed and improved our study- 🧠🧬🐁 #ATP1A3 #AHC
Novel mouse model of alternating hemiplegia of childhood