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[Mutations that map to the KvLQT1 and minK genes account for more than 50% of an inherited cardiac disorder, the Long QT syndrome (Splawski, I., Tristani-Firouzi, M., Lehmann, M. H., Sanguinetti, M. C., and Keating, M. T. (1997) Nat.Genet.17, 338-340).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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