Second Symposium on ATP1A3 in disease
Genotype/Phenotype Correlations, modelling and identification of potential targets for treatment
Catholic University School of Medicine
23 – 24 September 2013
The aim of the Symposium is to present the further progress of the research on Alternating Hemiplegia of Childhood (AHC), after the finding of the ATP1A3 gene as the primary cause of this rare neurological disease, to promote the international collaboration and recruit new teams of researchers.
Details Here: http://www.symposium-atp1a3.tk/