Article ISI
NATURE GENETICS  (2024)

Advancing diagnosis and research for rare genetic diseases in Indigenous peoples

Baynam, Gareth; Julkowska, Daria; Bowdin, Sarah; Hermes, Azure; McMaster, Christopher R.; Prichep, Elissa; Richer, Etienne; van der Westhuizen, Francois H.; Malherbe, Helen; Reichardt, Juergen K. V.; Arbour, Laura; Hudson, Maui; du Plessis, Kelly; Wilcox, Phillip; Rind, Shamir; et. al.

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.

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Título según WOS: ID WOS:001159368500001 Not found in local WOS DB
Título de la Revista: NATURE GENETICS
Editorial: NATURE PORTFOLIO
Fecha de publicación: 2024
DOI:

10.1038/s41588-023-01642-1
Notas: ISI