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Fine-Mapping Array Design for Multi-Ethnic Studies of Multiple Sclerosis
While approximately 200 autosomal genetic associations outside of the major histocompatibility complex (MHC) have been identified for multiple sclerosis (MS) risk in European populations, causal variants identified at the majority of these associated loci have been much more elusive. We propose that...
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| I publikationen: | Genes (Basel) |
|---|---|
| Huvudupphovsmän: | , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
MDPI
2019
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6895860/ https://ncbi.nlm.nih.gov/pubmed/31703377 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10110903 |
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