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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, E-ISSN 1652-7518, Vol. 104, no 40, p. 2866-2870Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2007. Vol. 104, no 40, p. 2866-2870
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, id: diva2:157818
Available from: 2008-06-26 Created: 2008-06-26 Last updated: 2017-12-14Bibliographically approved

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Jensen, SteenStattin, Eva-lena
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