Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes

Restless legs syndrome (RLS) is a common neurological condition, with a prevalence of 5–15% in Central Europe and North America. Although genome-wide association studies (GWAS) have identified some common risk regions for RLS, the causal genes have yet to be fully elucidated. We conducted a transcri...

Descripción completa

Detalles Bibliográficos
Autores principales: Akçimen, Fulya, Sarayloo, Faezeh, Liao, Calwing, Ross, Jay P., Oliveira, Rachel De Barros, Dion, Patrick A., Rouleau, Guy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351781/
https://www.ncbi.nlm.nih.gov/pubmed/32651461
http://dx.doi.org/10.1038/s42003-020-1105-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351781/
https://www.ncbi.nlm.nih.gov/pubmed/32651461
http://dx.doi.org/10.1038/s42003-020-1105-z

Ejemplares similares