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Advancing diagnosis and research for rare genetic diseases in Indigenous peoples
Journal article   Open access   Peer reviewed

Advancing diagnosis and research for rare genetic diseases in Indigenous peoples

Gareth Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R. McMaster, Elissa Prichep, Etienne Richer, Francois H. van der Westhuizen, Gabriela M. Repetto, Helen Malherbe, …
Nature genetics, Vol.56(2), pp.189-193
01/02/2024
Handle:
https://hdl.handle.net/10523/40705

Abstract

Genetics & Heredity Life Sciences & Biomedicine Science & Technology
Achieving a diagnosis for Indigenous people living with a rare, often genetic, disease is crucial for equitable healthcare. The International Rare Disease Research Consortium convened a global Task Force to bridge the gap in diagnosing Indigenous rare diseases, and identify solutions to tackle the health inequity faced by Indigenous people.
url
https://rdcu.be/dYMwbView
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