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Should variants of unknown significance (VUS) be disclosed to patients in cardiogenetics or not; only in case of high suspicion of pathogenicity?
Department of Clinical Genetics, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, Netherlands; European Reference Network for rare, low-prevalence, or complex diseases of the heart (ERN GUARD-Heart), Amsterdam, Netherlands.
Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine, Section of Medicine. European Reference Network for rare, low-prevalence, or complex diseases of the heart (ERN GUARD-Heart), Amsterdam, Netherlands.
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Paediatrics. European Reference Network for rare, low-prevalence, or complex diseases of the heart (ERN GUARD-Heart), Amsterdam, Netherlands.
Umeå University, Faculty of Medicine, Department of Medical Biosciences, Medical and Clinical Genetics. European Reference Network for rare, low-prevalence, or complex diseases of the heart (ERN GUARD-Heart), Amsterdam, Netherlands.
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2022 (English)In: European Journal of Human Genetics, ISSN 1018-4813, E-ISSN 1476-5438, Vol. 30, p. 1208-1210Article in journal, Editorial material (Refereed) Published
Place, publisher, year, edition, pages
Springer Nature, 2022. Vol. 30, p. 1208-1210
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Medical Genetics
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URN: urn:nbn:se:umu:diva-199393DOI: 10.1038/s41431-022-01173-zISI: 000844578000001PubMedID: 36008533Scopus ID: 2-s2.0-85137082057OAI: oai:DiVA.org:umu-199393DiVA, id: diva2:1699912
Available from: 2022-09-29 Created: 2022-09-29 Last updated: 2023-05-25Bibliographically approved

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Mörner, StellanLundström, AnnaJonasson, JenniRydberg, Annika

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