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

Original languageEnglish
JournalClinical Chemistry
Volume47
Issue number8
Pages (from-to)1390-1395
ISSN0009-9147
Publication statusPublished - 2001

ID: 122675