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Long-Read Sequencing: The Third Generation of Diagnostic Testing for Dystonia.

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Title: Long-Read Sequencing: The Third Generation of Diagnostic Testing for Dystonia.
Authors: Wirth T; Neurology Department, Strasbourg University Hospital, Strasbourg, France.; Institute of Genetics and of Molecular and Cellular Biology (IGBMC), INSERM-U964/CNRS-UMR7104/Strasbourg University, Illkirch-Graffenstaden, France.; Strasbourg Translational Medicine Federation (FMTS), Strasbourg University, Strasbourg, France., Kumar KR; Translational Neurogenomics Group, Genomics and Inherited Disease Program, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.; Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.; Department of Neurology and Molecular Medicine Laboratory, Concord Repatriation General Hospital, Concord, New South Wales, Australia.; School of Clinical Medicine, UNSW Medicine & Health, UNSW Sydney, Sydney, New South Wales, Australia., Zech M; Institute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.; Institute of Neurogenomics, Helmholtz Munich, Neuherberg, Germany.; Institute for Advanced Study, Technical University of Munich, Garching, Germany.
Source: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2025 Jun; Vol. 40 (6), pp. 1009-1019. Date of Electronic Publication: 2025 Apr 23.
Publication Type: Journal Article; Review
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: <searchLink fieldCode="AU" term="%22Wirth+T%22">Wirth T</searchLink>; Neurology Department, Strasbourg University Hospital, Strasbourg, France.; Institute of Genetics and of Molecular and Cellular Biology (IGBMC), INSERM-U964/CNRS-UMR7104/Strasbourg University, Illkirch-Graffenstaden, France.; Strasbourg Translational Medicine Federation (FMTS), Strasbourg University, Strasbourg, France.<br /><searchLink fieldCode="AU" term="%22Kumar+KR%22">Kumar KR</searchLink>; Translational Neurogenomics Group, Genomics and Inherited Disease Program, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.; Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.; Department of Neurology and Molecular Medicine Laboratory, Concord Repatriation General Hospital, Concord, New South Wales, Australia.; School of Clinical Medicine, UNSW Medicine & Health, UNSW Sydney, Sydney, New South Wales, Australia.<br /><searchLink fieldCode="AU" term="%22Zech+M%22">Zech M</searchLink>; Institute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.; Institute of Neurogenomics, Helmholtz Munich, Neuherberg, Germany.; Institute for Advanced Study, Technical University of Munich, Garching, Germany.
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  Data: <searchLink fieldCode="JN" term="%228610688%22">Movement disorders : official journal of the Movement Disorder Society</searchLink> [Mov Disord] 2025 Jun; Vol. 40 (6), pp. 1009-1019. <i>Date of Electronic Publication: </i>2025 Apr 23.
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        Value: 10.1002/mds.30208
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              Text: 2025 Jun
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