Exploring mutation carriers' preferences regarding onset and progression of disease predictions for adult-onset genetic neurodegenerative diseases: a qualitative interview study.

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Title: Exploring mutation carriers' preferences regarding onset and progression of disease predictions for adult-onset genetic neurodegenerative diseases: a qualitative interview study.
Authors: Rensink MJ; Medical Ethics, Philosophy and History of Medicine, Erasmus University Medical Centre, Dr. Molewaterplein 40, Rotterdam, 3015 GD, The Netherlands. m.rensink@erasmusmc.nl., Schermer MHN; Medical Ethics, Philosophy and History of Medicine, Erasmus University Medical Centre, Dr. Molewaterplein 40, Rotterdam, 3015 GD, The Netherlands., Tibben A; Department of Clinical Genetics, Leiden University Medical Center, Leiden, 2333 ZA, The Netherlands., Bijlsma EK; Department of Clinical Genetics, Leiden University Medical Center, Leiden, 2333 ZA, The Netherlands., de Bot ST; Department of Neurology, Leiden University Medical Center, Leiden, 2333 ZA, The Netherlands., Kievit JA; Department of Clinical Genetics, Erasmus University Medical Centre, Rotterdam, 3015 GD, The Netherlands., Bolt LLE; Medical Ethics, Philosophy and History of Medicine, Erasmus University Medical Centre, Dr. Molewaterplein 40, Rotterdam, 3015 GD, The Netherlands.
Source: Human genetics [Hum Genet] 2025 Jun; Vol. 144 (6), pp. 665-677. Date of Electronic Publication: 2025 May 26.
Publication Type: Journal Article
Journal Info: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE
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  Data: <searchLink fieldCode="AU" term="%22Rensink+MJ%22">Rensink MJ</searchLink>; Medical Ethics, Philosophy and History of Medicine, Erasmus University Medical Centre, Dr. Molewaterplein 40, Rotterdam, 3015 GD, The Netherlands. m.rensink@erasmusmc.nl.<br /><searchLink fieldCode="AU" term="%22Schermer+MHN%22">Schermer MHN</searchLink>; Medical Ethics, Philosophy and History of Medicine, Erasmus University Medical Centre, Dr. Molewaterplein 40, Rotterdam, 3015 GD, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Tibben+A%22">Tibben A</searchLink>; Department of Clinical Genetics, Leiden University Medical Center, Leiden, 2333 ZA, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Bijlsma+EK%22">Bijlsma EK</searchLink>; Department of Clinical Genetics, Leiden University Medical Center, Leiden, 2333 ZA, The Netherlands.<br /><searchLink fieldCode="AU" term="%22de+Bot+ST%22">de Bot ST</searchLink>; Department of Neurology, Leiden University Medical Center, Leiden, 2333 ZA, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Kievit+JA%22">Kievit JA</searchLink>; Department of Clinical Genetics, Erasmus University Medical Centre, Rotterdam, 3015 GD, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Bolt+LLE%22">Bolt LLE</searchLink>; Medical Ethics, Philosophy and History of Medicine, Erasmus University Medical Centre, Dr. Molewaterplein 40, Rotterdam, 3015 GD, The Netherlands.
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  Data: <searchLink fieldCode="JN" term="%227613873%22">Human genetics</searchLink> [Hum Genet] 2025 Jun; Vol. 144 (6), pp. 665-677. <i>Date of Electronic Publication: </i>2025 May 26.
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        Value: 10.1007/s00439-025-02750-0
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              Text: 2025 Jun
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