Referral route: a determinant of inequity for children with undiagnosed genetic diseases?
Individuals with rare genetic diseases collectively comprise 3.5%–5.9% of the population, roughly 400 million people worldwide. Undiagnosed rare disease programs have leveraged next-generation sequencing technologies to facilitate genetic diagnoses, thereby shortening the complex diagnostic odysseys...
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| Autores principales: | , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Frontiers Media S.A.
2026-01-01
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| Colección: | Frontiers in Genetics |
| Materias: | |
| Acceso en línea: | https://www.frontiersin.org/articles/10.3389/fgene.2026.1692489/full |
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