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Filtern nach: Platform Presentation Yes, please Study Program Human Genetics and Genomics Study Program (HGSP)

1. Investigating the Relationship Between Heart Rate, QT, and QTc in Alternating Hemiplegia of Childhood and Other ATP1A3-Associated Phenotypes

Beschreibung:: Background: Alternating hemiplegia of childhood (AHC) is a rare condition most frequently caused by mutations in ATP1A3, encoding for the alpha-3 subunit of Na+/K+-ATPase, and D801N is the most common variant. Individuals with ATP1A3-D801N have shorter...
Datum erstellt:: August 1-2, 2024