Preferences for genetic interventions for SCA and Huntington’s disease: results of a discrete choice experiment among patients
The results can be used for the design and implementation of future genetic interventional trials as well as of patient-centered care pathways for rare movement disorders such as SCA and HD.
Authors
- Bart P.C. van de Warrenburg (ORCID: https://orcid.org/0000-0003-4412-1616)
- Brigitte A.B. Essers (ORCID: https://orcid.org/0000-0002-7703-7114)
- Mayke Oosterloo (ORCID: https://orcid.org/0000-0003-0732-4406)
- Nienke J.H. van Os (ORCID: https://orcid.org/0000-0003-4266-7164)
- Janneke P.C. Grutters (ORCID: https://orcid.org/0000-0002-2579-1561)
Institutions
- Radboud University Nijmegen (NL)
- Maastricht University Medical Centre (NL)
- Radboud University Medical Center (NL)
- Maastricht University (NL)
- Radboud Institute for Molecular Life Sciences (NL)
Publication Details
- Journal
- Orphanet Journal of Rare Diseases
- Published
- 2024-10-28
- DOI
- https://doi.org/10.1186/s13023-024-03408-2
- Citations
- 2
- Primary Topic
- Genetic Neurodegenerative Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.54
Funders
- Maastricht Universitair Medisch Centrum
- Radboud Universitair Medisch Centrum