Cargando…
Solving unsolved rare neurological diseases—a Solve-RD viewpoint
Autores principales: | Schüle, Rebecca, Timmann, Dagmar, Erasmus, Corrie E., Reichbauer, Jennifer, Wayand, Melanie, van de Warrenburg, Bart, Schöls, Ludger, Wilke, Carlo, Bevot, Andrea, Zuchner, Stephan, Beltran, Sergi, Laurie, Steven, Matalonga, Leslie, Graessner, Holm, Synofzik, Matthis |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440537/ https://www.ncbi.nlm.nih.gov/pubmed/33972714 http://dx.doi.org/10.1038/s41431-021-00901-1 |
Ejemplares similares
-
Solving the unsolved rare diseases in Europe
por: Graessner, Holm, et al.
Publicado: (2021) -
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
por: Zurek, Birte, et al.
Publicado: (2021) -
Uniparental disomy determined by whole‐exome sequencing in a spectrum of rare motoneuron diseases and ataxias
por: Bis, Dana M., et al.
Publicado: (2017) -
Ambulance Problems Solved and Unsolved
Publicado: (1914) -
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data
por: Matalonga, Leslie, et al.
Publicado: (2021)