Finding commonalities in rare diseases through the undiagnosed diseases network

OBJECTIVE: When studying any specific rare disease, heterogeneity and scarcity of affected individuals has historically hindered investigators from discerning on what to focus to understand and diagnose a disease. New nongenomic methodologies must be developed that identify similarities in seemingly...

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Detalles Bibliográficos
Autores principales: Yates, Josephine, Gutiérrez-Sacristán, Alba, Jouhet, Vianney, LeBlanc, Kimberly, Esteves, Cecilia, DeSain, Thomas N, Benik, Nick, Stedman, Jason, Palmer, Nathan, Mellon, Guillaume, Kohane, Isaac, Avillach, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Research and Applications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8324228/
https://www.ncbi.nlm.nih.gov/pubmed/34009343
http://dx.doi.org/10.1093/jamia/ocab050

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8324228/
https://www.ncbi.nlm.nih.gov/pubmed/34009343
http://dx.doi.org/10.1093/jamia/ocab050

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