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[Long QT syndrome can be effectively treated. Important to identify mutation carriers]
Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine. (Kardiologi)
Umeå University, Faculty of Medicine, Department of Medical Biosciences, Medical and Clinical Genetics.
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Paediatrics.
2007 (English)In: Läkartidningen, ISSN 0023-7205, Vol. 104, no 40, 2866-2870 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2007. Vol. 104, no 40, 2866-2870 p.
Keyword [en]
Adrenergic beta-Antagonists/therapeutic use, Adult, Child, Child; Preschool, Female, Genetic Techniques, Heterozygote Detection, Humans, Infant, Long QT Syndrome/diagnosis/drug therapy/genetics, Male, Mutation; Missense, Pedigree, Pregnancy, Prenatal Diagnosis, Prognosis, Risk Assessment
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Medical and Health Sciences
Identifiers
URN: urn:nbn:se:umu:diva-18145PubMedID: 17966800OAI: oai:DiVA.org:umu-18145DiVA: diva2:157818
Available from: 2008-06-26 Created: 2008-06-26 Last updated: 2011-01-19Bibliographically approved

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Jensen, SteenStattin, Eva-lena

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