Detalle de: CrinGenES: genomic newborn screening for rare diseases
| Title | CrinGenES: genomic newborn screening for rare diseases |
| Description |
Pilot of genomic newborn screening (whole-genome sequencing) in 2,500 newborns from nine Spanish regions, to detect more than 300 treatable paediatric-onset rare diseases. Funded by the ISCIII with NextGenerationEU funds (2.4 M€ for the whole consortium); led by María Luz Couce and Miguel Ángel Moreno Pelayo. María de Toro (CIBIR): participant (La Rioja). |
| Type Of Funding | |
| Funding Agency | Instituto de Salud Carlos III (ISCIII) - NextGenerationEU |
| Grant Number | |
| Project Acronym | CRINGENES |
| Period | 2025 – 2026 |
| Funding Amount | |
| Ontology | |
| Research Groups | |
| Researchers | María de Toro |