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 was 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.
To download the Brochure of the Symposium click here
To read the Concluding Remarks of Dr. David Goldstein
The Sixth Edition of the Symposium on ATP1A3 in disease
will be held at the
Hotel Tachikawa, Tachikawa City
21 – 22 September 2017
National Center of Neurology and Psychiatry
Japan AHC Family Association (JAFA)
Japanese Society of Child Neurology
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