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Dive into the research topics of 'Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2'. Together they form a unique fingerprint.- Sort by
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Michael Christiansen, Paula L. Hedley, Juliane Theilade, Birgitte Stoevring, Trond P. Leren, Ole Eschen, Karina M. Sørensen, Anne Tybjærg-Hansen, Lilian B. Ousager, Lisbeth N. Pedersen, Ruth Frikke-Schmidt, Frederik H. Aidt, Michael G Hansen, Jim Hansen, Poul E Bloch Thomsen, Egon Toft, Finn L Henriksen, Henning Bundgaard, Henrik K Jensen, Jørgen K. Kanters