Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2
丹麦长QT综合征患者的基因突变以及KCNH2基因p.F29L突变的大型创始家族的鉴定
期刊:BMC Medical Genetics
影响因子:
doi:10.1186/1471-2350-15-31
Christiansen, Michael; Hedley, Paula L; Theilade, Juliane; Stoevring, Birgitte; Leren, Trond P; Eschen, Ole; Sørensen, Karina M; Tybjærg-Hansen, Anne; Ousager, Lilian B; Pedersen, Lisbeth N; Frikke-Schmidt, Ruth; Aidt, Frederik H; Hansen, Michael G; Hansen, Jim; Bloch Thomsen, Poul E; Toft, Egon; Henriksen, Finn L; Bundgaard, Henning; Jensen, Henrik K; Kanters, Jørgen K
