Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome

Research output: Contribution to journalJournal articleResearchpeer-review

Lars Allan Larsen, Paal Skytt Andersen, Jørgen K. Kanters, Ida Hastrup Svendsen, J.R. Jacobsen, J. Vuust, G. Wetrell, Lisbeth Tranebjærg, M. Christiansen

Original languageEnglish
JournalClinical Chemistry
Issue number8
Pages (from-to)1390-1395
Publication statusPublished - 2001

ID: 122675