Academic Journal
Advancing diagnosis and research for rare genetic diseases in indigenous peoples
العنوان: | Advancing diagnosis and research for rare genetic diseases in indigenous peoples |
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المؤلفون: | Baynam, Gareth, Julkowska, Daria, Bowdin, Sarah, Hermes, Azure, McMaster, Christopher R., Prichep, Elissa, Richer, Etienne, Van der Westhuizen, Francois H., Repetto, Gabriela M., Malherbe, Helen L., Reichardt, Juergen K.V., Arbour, Laura, Hudson, Maui, Du Plessis, Kelly, Haendel, Melissa, Wilcox, Phillip, Lynch, Sally Ann, Rind, Shamir, Easteal, Simon, Estivill, Xavier, Caron, Nadine, Chongo, Meck, Thomas, Yarlalu, Letinturier, Mary Catherine V., Vorster, Barend Christiaan |
بيانات النشر: | Nature Research |
سنة النشر: | 2024 |
المجموعة: | University of Pretoria: UPSpace |
مصطلحات موضوعية: | Genetic services, Genetics research, Indigenous people, Healthcare, Rare diseases, Genetic diseases, SDG-03: Good health and well-being, Indigenous rare diseases, Health inequity, SDG-10: Reduced inequalities |
الوصف: | 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. ; The IRDiRC Indigenous Population Task Force was supported by the Scientific Secretariat of IRDiRC, funded by the European Union through the European Joint Programme on Rare Disease (EJP RD) under the European Union’s Horizon 2020 Research and Innovation Programme. ; https://www.nature.com/ng ; 2024-08-08 ; hj2024 ; Biochemistry ; Genetics ; Microbiology and Plant Pathology ; SDG-03:Good heatlh and well-being ; SDG-10:Reduces inequalities |
نوع الوثيقة: | article in journal/newspaper |
وصف الملف: | application/pdf |
اللغة: | English |
Relation: | Baynam, G., Julkowska, D., Bowdin, S. et al. Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature Genetics 56, 189–193 (2024). https://doi.org/10.1038/s41588-023-01642-1.; 1061-4036 (print); 1546-1718 (online); http://hdl.handle.net/2263/96770 |
DOI: | 10.1038/s41588-023-01642-1 |
الاتاحة: | http://hdl.handle.net/2263/96770 https://doi.org/10.1038/s41588-023-01642-1 |
Rights: | © 2024, The Author(s), under exclusive licence to Springer Nature America, Inc. |
رقم الانضمام: | edsbas.9DE7FEA9 |
قاعدة البيانات: | BASE |
DOI: | 10.1038/s41588-023-01642-1 |
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