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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...
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| Publicado no: | Commun Biol |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7351781/ https://ncbi.nlm.nih.gov/pubmed/32651461 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s42003-020-1105-z |
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