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2007The common Long QT Syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.Crotti L; Spazzolini C; Schwartz Pj; Shimizu W; Denjoy I; Schulze bahr E; Zaklyazminskaya Ev; Swan H; Ackerman MJ; Moss AJ; Wilde AA; Horie M; Brink Pa; Insolia R; De Ferrari GM; Crimi G
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