Publication: Advancing diagnosis and research for rare genetic diseases in Indigenous peoples
dc.contributor.author | Baynam, Gareth | |
dc.contributor.author | Julkowska, Daria | |
dc.contributor.author | Bowdin, Sarah | |
dc.contributor.author | Hermes, Azure | |
dc.contributor.author | McMaster, Christopher | |
dc.contributor.author | Prichep, Elissa | |
dc.contributor.author | Richer, Étienne | |
dc.contributor.author | Van der Westhuizen, Francois | |
dc.contributor.author | Repetto, Gabriela | |
dc.contributor.author | Malherbe, Helen | |
dc.contributor.author | Reichardt, Juergen | |
dc.contributor.author | Arbour, Laura | |
dc.contributor.author | Hudson, Maui | |
dc.contributor.author | Du Plessis, Kelly | |
dc.contributor.author | Haendel, Melissa | |
dc.contributor.author | Wilcox, Phillip | |
dc.contributor.author | Lynch, Sally | |
dc.contributor.author | Rind, Shamir | |
dc.contributor.author | Easteal, Simon | |
dc.contributor.author | Estivill, Xavier | |
dc.contributor.author | Caron, Nadine | |
dc.contributor.author | Chongo, Meck | |
dc.contributor.author | Thomas, Yarlalu | |
dc.contributor.author | Letinturier, Mary | |
dc.contributor.author | Vorster. Barend | |
dc.date.accessioned | 2025-01-09T16:13:00Z | |
dc.date.available | 2025-01-09T16:13:00Z | |
dc.date.issued | 2024 | |
dc.description.abstract | 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. | |
dc.description.version | Versión Aceptada | |
dc.identifier.citation | Baynam G, Julkowska D, Bowdin S, Hermes A, McMaster CR, Prichep E, Richer É, van der Westhuizen FH, Repetto GM, Malherbe H, Reichardt JKV, Arbour L, Hudson M, du Plessis K, Haendel M, Wilcox P, Lynch SA, Rind S, Easteal S, Estivill X, Caron N, Chongo M, Thomas Y, Letinturier MCV, Vorster BC. Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nat Genet. 2024 Feb;56(2):189-193. doi: 10.1038/s41588-023-01642-1 | |
dc.identifier.doi | https://doi.org/10.1038/s41588-023-01642-1 | |
dc.identifier.uri | https://hdl.handle.net/11447/9605 | |
dc.language.iso | en | |
dc.title | Advancing diagnosis and research for rare genetic diseases in Indigenous peoples | |
dc.type | Article | |
dcterms.accessRights | Acceso Abierto | |
dcterms.source | Nature genetics | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | 98c75303-d87e-4c17-9d27-d9d710229223 | |
relation.isAuthorOfPublication.latestForDiscovery | 98c75303-d87e-4c17-9d27-d9d710229223 |
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