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pro vyhledávání: '"Heikki Mäkynen M.D."'
Autor:
Heikki Mäkynen M.D., Pekka Mäkynen, Vesa Virtanen M.D., Katriina Aalto-Setälä, Sinikka Yli-Mäyry M.D., Kimmo Kontula, Päivi J. Laitinen-Forsblom
Publikováno v:
Journal of Cardiovascular Electrophysiology. 17:480-485
SCN5A Mutation. Introduction: We aimed at identifying the molecular defect underlying the clinical phenotype of a Finnish family with a cardiac conduction defect and atrial arrhythmias. Methods and Results: A large Finnish family was clinically evalu