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Huntington's Disease and Huntington's Disease-like 2 (HDL2) in Martinique.

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Title: Huntington's Disease and Huntington's Disease-like 2 (HDL2) in Martinique.
Authors: Antolin-Sanfeliz I; Centre de Référence Caribéen des Maladies Neuromusculaires Rares, CHU de Martinique, Fort-de-France, France., Giguet-Valard AG; Centre de Référence Caribéen des Maladies Neuromusculaires Rares, CHU de Martinique, Fort-de-France, France., Duclos S; Centre de Référence Caribéen des Maladies Neuromusculaires Rares, CHU de Martinique, Fort-de-France, France., Cazeneuve C; UF de Neurogénétique Moléculaire et Cellulaire, Département de Génétique, Hôpitaux Universitaires Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, Paris, France., Angelini C; Centre de Référence Maladies Rares 'Maladie De Huntington Et Autres Chorées' and Centre de référence maladies rares 'Neurogénétique', Service de Génétique Médicale, Bordeaux University Hospital (CHU Bordeaux) and Univ. Bordeaux, CNRS, INCIA, UMR 5287, EPHE, Bordeaux, France., Signaté A; Centre de Référence Caribéen des Maladies Neuromusculaires Rares, CHU de Martinique, Fort-de-France, France., Margolis RL; Division of Neurobiology, Department of Psychiatry and Behavioral Sciences, and Department of Neurology, John Hopkins University School of Medicine, Baltimore, Maryland, USA., Goizet C; Centre de Référence Maladies Rares 'Maladie De Huntington Et Autres Chorées' and Centre de référence maladies rares 'Neurogénétique', Service de Génétique Médicale, Bordeaux University Hospital (CHU Bordeaux) and Univ. Bordeaux, CNRS, INCIA, UMR 5287, EPHE, Bordeaux, France., Bellance R; Centre de Référence Caribéen des Maladies Neuromusculaires Rares, CHU de Martinique, Fort-de-France, France.
Source: Movement disorders clinical practice [Mov Disord Clin Pract] 2026 Mar; Vol. 13 (3), pp. 673-682. Date of Electronic Publication: 2025 Oct 11.
Publication Type: Journal Article
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 101630279 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2330-1619 (Electronic) Linking ISSN: 23301619 NLM ISO Abbreviation: Mov Disord Clin Pract Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Huntington's Disease and Huntington's Disease-like 2 (HDL2) in Martinique.
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  Data: <searchLink fieldCode="AU" term="%22Antolin-Sanfeliz+I%22">Antolin-Sanfeliz I</searchLink>; Centre de Référence Caribéen des Maladies Neuromusculaires Rares, CHU de Martinique, Fort-de-France, France.<br /><searchLink fieldCode="AU" term="%22Giguet-Valard+AG%22">Giguet-Valard AG</searchLink>; Centre de Référence Caribéen des Maladies Neuromusculaires Rares, CHU de Martinique, Fort-de-France, France.<br /><searchLink fieldCode="AU" term="%22Duclos+S%22">Duclos S</searchLink>; Centre de Référence Caribéen des Maladies Neuromusculaires Rares, CHU de Martinique, Fort-de-France, France.<br /><searchLink fieldCode="AU" term="%22Cazeneuve+C%22">Cazeneuve C</searchLink>; UF de Neurogénétique Moléculaire et Cellulaire, Département de Génétique, Hôpitaux Universitaires Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, Paris, France.<br /><searchLink fieldCode="AU" term="%22Angelini+C%22">Angelini C</searchLink>; Centre de Référence Maladies Rares 'Maladie De Huntington Et Autres Chorées' and Centre de référence maladies rares 'Neurogénétique', Service de Génétique Médicale, Bordeaux University Hospital (CHU Bordeaux) and Univ. Bordeaux, CNRS, INCIA, UMR 5287, EPHE, Bordeaux, France.<br /><searchLink fieldCode="AU" term="%22Signaté+A%22">Signaté A</searchLink>; Centre de Référence Caribéen des Maladies Neuromusculaires Rares, CHU de Martinique, Fort-de-France, France.<br /><searchLink fieldCode="AU" term="%22Margolis+RL%22">Margolis RL</searchLink>; Division of Neurobiology, Department of Psychiatry and Behavioral Sciences, and Department of Neurology, John Hopkins University School of Medicine, Baltimore, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Goizet+C%22">Goizet C</searchLink>; Centre de Référence Maladies Rares 'Maladie De Huntington Et Autres Chorées' and Centre de référence maladies rares 'Neurogénétique', Service de Génétique Médicale, Bordeaux University Hospital (CHU Bordeaux) and Univ. Bordeaux, CNRS, INCIA, UMR 5287, EPHE, Bordeaux, France.<br /><searchLink fieldCode="AU" term="%22Bellance+R%22">Bellance R</searchLink>; Centre de Référence Caribéen des Maladies Neuromusculaires Rares, CHU de Martinique, Fort-de-France, France.
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  Data: <searchLink fieldCode="JN" term="%22101630279%22">Movement disorders clinical practice</searchLink> [Mov Disord Clin Pract] 2026 Mar; Vol. 13 (3), pp. 673-682. <i>Date of Electronic Publication: </i>2025 Oct 11.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley%22">Wiley </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101630279 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2330-1619 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2223301619%22">23301619 </searchLink><i>NLM ISO Abbreviation: </i>Mov Disord Clin Pract <i>Subsets: </i>MEDLINE
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        Value: 10.1002/mdc3.70379
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        Text: English
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              Text: 2026 Mar
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