RDmap: a map for exploring rare diseases

BACKGROUND: The complexity of the phenotypic characteristics and molecular bases of many rare human genetic diseases makes the diagnosis of such diseases a challenge for clinicians. A map for visualizing, locating and navigating rare diseases based on similarity will help clinicians and researchers...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Jian, Dong, Cong, Duan, Huilong, Shu, Qiang, Li, Haomin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905868/
https://www.ncbi.nlm.nih.gov/pubmed/33632281
http://dx.doi.org/10.1186/s13023-021-01741-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905868/
https://www.ncbi.nlm.nih.gov/pubmed/33632281
http://dx.doi.org/10.1186/s13023-021-01741-4

Ejemplares similares