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    • Clinical disease presentation and ECG characteristics of LMNA mutation carriers 

      Ollila L; Nikus K; Holmström M; Jalanko M; Jurkko R; Kaartinen M; Koskenvuo J; Kuusisto J; Kärkkäinen S; Palojoki E; Reissell E; Piirilä P; Heliö T (2017)
      Objective Mutations in the LMNA gene encoding lamins A and C of the nuclear lamina are a frequent cause of cardiomyopathy accounting for 5–8% of familial dilated cardiomyopathy (DCM). Our aim was to study disease onset, ...