Harvard Catalyst Profiles

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

Identification of a Kir3.4 Mutation in Congenital Long QT Syndrome.

Identification of a Kir3.4 Mutation in Congenital Long QT Syndrome. Am J Hum Genet. 2010 Jun 2.

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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.