Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nat Genet. 2012 Sep; 44(9):1030-4.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.