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NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk
A recent study by Wang et al. (2016a) claims that the low-frequency variant NR1H3 p.Arg415Gln is sufficient to cause multiple sclerosis in certain individuals and determines a patient’s likelihood of primary progressive disease. We sought to replicate this finding in the International MS Genetics Co...
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| Publicado no: | Neuron |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5641967/ https://ncbi.nlm.nih.gov/pubmed/27764667 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2016.09.052 |
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