Claudia Stöllberger, Josef Finsterer. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Cardiomyopathies/geneticsCardiomyopathies/physiopathologyChannelopathies/geneticsChannelopathies/physiopathologyDefibrillators, ImplantableHumansInfantKCNQ1 Potassium Channel/geneticsLong QT Syndrome/geneticsLong QT Syndrome/therapyMutation
Substances: See more » KCNQ1 Potassium ChannelKCNQ1 protein, human
Year: 2012 PMID: 22706706 DOI: 10.1007/s00246-012-0410-9
Source DB: PubMed Journal: Pediatr Cardiol ISSN: 0172-0643 Impact factor: 1.655