Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.
Christiansen M, Hedley PL, Theilade J, Stoevring B, Leren TP, Eschen O, Sørensen KM, Tybjærg-Hansen A, Ousager LB, Pedersen LN, Frikke-Schmidt R, Aidt FH, Hansen MG, Hansen J, Bloch Thomsen PE, Toft E, Henriksen FL, Bundgaard H, Jensen HK, Kanters JK.
Christiansen M, et al.
BMC Med Genet. 2014 Mar 7;15:31. doi: 10.1186/1471-2350-15-31.
BMC Med Genet. 2014.
PMID: 24606995
Free PMC article.