Title : Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypes.

Pub. Date : 2014 Dec

PMID : 25439493






1 Functional Relationships(s)
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1 PATIENT: We present a child with topiramate-responsive alternating hemiplegia of childhood who was tested for an ATP1A3 gene mutation. Topiramate ATPase Na+/K+ transporting subunit alpha 3 Homo sapiens