Huntington's Disease and Huntington's Disease‐like 2 ( <scp>HDL2</scp> ) in Martinique
HDL2 is nearly as prevalent as HD in Martinique. The study reinforces the similarities between HD and HDL2 in genotype-phenotype correlation and disease course, while highlighting heterogeneity and germline instability in HDL2. Interpretation is limited by the small number of HDL2 families.
Authors
- Anna‐Gaëlle Giguet‐Valard (ORCID: https://orcid.org/0000-0003-2260-2021)
- Chloé Angelini (ORCID: https://orcid.org/0000-0002-5825-5319)
- Cyril Goizet (ORCID: https://orcid.org/0000-0002-1913-889X)
- Aïssatou Signaté (ORCID: https://orcid.org/0000-0001-7857-386X)
- Sophie Duclos
- Russell L. Margolis (ORCID: https://orcid.org/0000-0003-3024-8595)
- Cécile Cazeneuve (ORCID: https://orcid.org/0000-0002-5195-9348)
- Rémi Bellance (ORCID: https://orcid.org/0000-0002-6093-0838)
- Ignacio Antolin‐Sanfeliz
Institutions
- Centre National de la Recherche Scientifique (FR)
- Johns Hopkins University (US)
- Université de Bordeaux (FR)
- École Pratique des Hautes Études (FR)
- Johns Hopkins Medicine (US)
- Centre Hospitalier Universitaire de Bordeaux (FR)
- Assistance Publique – Hôpitaux de Paris (FR)
- Behavioral Pharma (United States) (US)
- Institut de Neurosciences Cognitives et Intégratives d’Aquitaine (FR)
- Centre Hospitalier Universitaire de Martinique (MQ)
Publication Details
- Journal
- Movement Disorders Clinical Practice
- Published
- 2025-10-11
- DOI
- https://doi.org/10.1002/mdc3.70379
- Primary Topic
- Genetic Neurodegenerative Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- University Hospital of Martinique