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Journal article : Review

Preclinical research (on rare diseases): we need to talk about health equity

Abstract:
There is a thriving, worldwide, biomedical research community working to understand the molecular bases of diseases of all types, continuously driving improved diagnostics and therapies. Developments in genetics and experimental medicine are yielding novel genetic therapies that were hardly dreamt of 40 years ago. But along with these scientific achievements, there exist challenges in ensuring that 21st century medical interventions are accessible to all who need them. This perspective will discuss how preclinical research, with a focus on rare diseases, can better contribute to healthcare ecosystems that are oriented towards greater health equity. This contribution may require changes to the prevailing scientific research culture that will need support from relevant institutions and the wider community.
Publication status:
Published
Peer review status:
Peer reviewed

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Files:
Publisher copy:
10.1007/s00335-024-10080-1

Authors


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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-1477-1776


Publisher:
Springer
Journal:
Mammalian Genome More from this journal
Volume:
36
Issue:
2
Pages:
347-353
Publication date:
2024-10-26
Acceptance date:
2024-10-21
DOI:
EISSN:
1432-1777
ISSN:
0938-8990


Language:
English
Keywords:
Subtype:
Review
Source identifiers:
2994668
Deposit date:
2025-06-03
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