Sequence Variants in Small CAG Repeat Expansions of the HTT Gene and Disease Onset and Progression in Huntington Disease.
Saved in:
| Title: | Sequence Variants in Small CAG Repeat Expansions of the HTT Gene and Disease Onset and Progression in Huntington Disease. |
|---|---|
| Authors: | Heinzmann A; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France., Petit E; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France., Dawson J; Center for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, Canada., Kay C; Center for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, Canada., Davoine CS; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France., Méreaux JL; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France., Black HF; Center for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, Canada., Arning L; Department of Human Genetics, Medical Faculty, Ruhr University of Bochum, Germany., Nguyen HP; Department of Human Genetics, Medical Faculty, Ruhr University of Bochum, Germany., Coarelli G; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France., Sayah S; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France., Pariente J; Neurology Department, Hôpital Purpan, Centre Hospitalier Universitaire de Toulouse, France; and.; Toulouse NeuroImaging Center (ToNIC), INSERM-University of Toulouse Paul Sabatier, France., Gérard F; Neurology Department, Hôpital Purpan, Centre Hospitalier Universitaire de Toulouse, France; and., Hurmic H; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France., Hayden MR; Center for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, Canada., Durr A; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France. |
| Source: | Neurology [Neurology] 2026 Jan 13; Vol. 106 (1), pp. e214404. Date of Electronic Publication: 2025 Dec 19. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1526-632X (Electronic) Linking ISSN: 00283878 NLM ISO Abbreviation: Neurology Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41418088 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Sequence Variants in Small CAG Repeat Expansions of the HTT Gene and Disease Onset and Progression in Huntington Disease. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Heinzmann+A%22">Heinzmann A</searchLink>; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France.<br /><searchLink fieldCode="AU" term="%22Petit+E%22">Petit E</searchLink>; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France.<br /><searchLink fieldCode="AU" term="%22Dawson+J%22">Dawson J</searchLink>; Center for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, Canada.<br /><searchLink fieldCode="AU" term="%22Kay+C%22">Kay C</searchLink>; Center for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, Canada.<br /><searchLink fieldCode="AU" term="%22Davoine+CS%22">Davoine CS</searchLink>; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France.<br /><searchLink fieldCode="AU" term="%22Méreaux+JL%22">Méreaux JL</searchLink>; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France.<br /><searchLink fieldCode="AU" term="%22Black+HF%22">Black HF</searchLink>; Center for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, Canada.<br /><searchLink fieldCode="AU" term="%22Arning+L%22">Arning L</searchLink>; Department of Human Genetics, Medical Faculty, Ruhr University of Bochum, Germany.<br /><searchLink fieldCode="AU" term="%22Nguyen+HP%22">Nguyen HP</searchLink>; Department of Human Genetics, Medical Faculty, Ruhr University of Bochum, Germany.<br /><searchLink fieldCode="AU" term="%22Coarelli+G%22">Coarelli G</searchLink>; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France.<br /><searchLink fieldCode="AU" term="%22Sayah+S%22">Sayah S</searchLink>; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France.<br /><searchLink fieldCode="AU" term="%22Pariente+J%22">Pariente J</searchLink>; Neurology Department, Hôpital Purpan, Centre Hospitalier Universitaire de Toulouse, France; and.; Toulouse NeuroImaging Center (ToNIC), INSERM-University of Toulouse Paul Sabatier, France.<br /><searchLink fieldCode="AU" term="%22Gérard+F%22">Gérard F</searchLink>; Neurology Department, Hôpital Purpan, Centre Hospitalier Universitaire de Toulouse, France; and.<br /><searchLink fieldCode="AU" term="%22Hurmic+H%22">Hurmic H</searchLink>; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France.<br /><searchLink fieldCode="AU" term="%22Hayden+MR%22">Hayden MR</searchLink>; Center for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, Canada.<br /><searchLink fieldCode="AU" term="%22Durr+A%22">Durr A</searchLink>; Sorbonne Université, Paris Brain Institute (ICM Institut du Cerveau), APHP, INSERM, CRNS, France. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220401060%22">Neurology</searchLink> [Neurology] 2026 Jan 13; Vol. 106 (1), pp. e214404. <i>Date of Electronic Publication: </i>2025 Dec 19. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lippincott+Williams+%26+Wilkins%22">Lippincott Williams & Wilkins </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0401060 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1526-632X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200283878%22">00283878 </searchLink><i>NLM ISO Abbreviation: </i>Neurology <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41418088 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1212/WNL.0000000000214404 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: e214404 Titles: – TitleFull: Sequence Variants in Small CAG Repeat Expansions of the HTT Gene and Disease Onset and Progression in Huntington Disease. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Heinzmann A – PersonEntity: Name: NameFull: Petit E – PersonEntity: Name: NameFull: Dawson J – PersonEntity: Name: NameFull: Kay C – PersonEntity: Name: NameFull: Davoine CS – PersonEntity: Name: NameFull: Méreaux JL – PersonEntity: Name: NameFull: Black HF – PersonEntity: Name: NameFull: Arning L – PersonEntity: Name: NameFull: Nguyen HP – PersonEntity: Name: NameFull: Coarelli G – PersonEntity: Name: NameFull: Sayah S – PersonEntity: Name: NameFull: Pariente J – PersonEntity: Name: NameFull: Gérard F – PersonEntity: Name: NameFull: Hurmic H – PersonEntity: Name: NameFull: Hayden MR – PersonEntity: Name: NameFull: Durr A IsPartOfRelationships: – BibEntity: Dates: – D: 13 M: 01 Text: 2026 Jan 13 Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1526-632X Numbering: – Type: volume Value: 106 – Type: issue Value: 1 Titles: – TitleFull: Neurology Type: main |
| ResultId | 1 |