Subject
Now showing items 1-1 of 1
-
Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2
(BioMed Central, 2014-03)Background: Long QT syndrome (LQTS) is a cardiac ion channelopathy which presents clinically with palpitations, syncope or sudden death. More than 700 LQTS-causing mutations have been identified in 13 genes, all of which ...