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Advancing diagnosis and research for rare genetic diseases in Indigenous peoples

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dc.contributor.authorBaynam, Gareth
dc.contributor.authorJulkowska, Daria
dc.contributor.authorBowdin, Sarah
dc.contributor.authorHermes, Azure
dc.contributor.authorMcMaster, Christopher R.
dc.contributor.authorPrichep, Elissa
dc.contributor.authorRicher, Étienne
dc.contributor.authorvan der Westhuizen, Francois H.
dc.contributor.authorRepetto, Gabriela M.
dc.contributor.authorMalherbe, Helen
dc.contributor.authorReichardt, Juergen K. V.
dc.contributor.authorArbour, Laura
dc.contributor.authorHudson, Maui
dc.contributor.authordu Plessis, Kelly
dc.contributor.authorHaendel, Melissa
dc.contributor.authorWilcox, Phillip
dc.contributor.authorLynch, Sally Ann
dc.contributor.authorRind, Shamir
dc.contributor.authorEasteal, Simon
dc.contributor.authorEstivill, Xavier
dc.contributor.authorCaron, Nadine
dc.contributor.authorChongo, Meck
dc.contributor.authorThomas, Yarlalu
dc.contributor.authorLetinturier, Mary Catherine V.
dc.contributor.authorVorster, Barend Christiaan
dc.date.accessioned2026-01-07T09:08:46Z
dc.date.issued2024
dc.descriptionJournal Article, Human Metabolomics, North-West University, Potchefstroom,
dc.description.abstractAchieving 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.
dc.identifier.citationaynam, G et al. 2024. Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nat Genet 56, 189–193 . https://doi.org/10.1038/s41588-023-01642-1
dc.identifier.urihttp://hdl.handle.net/10394/44948
dc.language.isoen
dc.publisherNature Publishing Group
dc.titleAdvancing diagnosis and research for rare genetic diseases in Indigenous peoples
dc.typeArticle

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