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. |
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| 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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| ISSN: | 1531-8257 |
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| DOI: | 10.1002/mds.30208 |
