Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRPI ion channel: Implications for acquired and congenital long Q-T syndrome

L. A. Larsen, P. S. Andersen, J. Kanters, I. H. Svendsen, J. R. Jacobsen, J. Vuust, G. Wettrell, L. TranebjÆrg, J. Bathen, M. Christiansen*

*Corresponding author af dette arbejde
66 Citationer (Scopus)

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Medicin og biovidenskab