Nuclear receptor NR1H3 in familial multiple sclerosis

Multiple sclerosis (MS) is an inflammatory disease characterized by myelin loss and neuronal dysfunction. Despite the aggregation observed in some families, pathogenic mutations have remained elusive. In this study we describe the identification of NR1H3 p.Arg415Gln in seven MS patients from two mul...

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Detalhes bibliográficos
Publicado no:Neuron
Main Authors: Wang, Zhe, Sadovnick, A. Dessa, Traboulsee, Anthony L., Ross, Jay P., Bernales, Cecily Q., Encarnacion, Mary, Yee, Irene M., de Lemos, Madonna, Greenwood, Talitha, Lee, Joshua D., Wright, Galen, Ross, Colin J., Zhang, Si, Song, Weihong, Vilariño-Güell, Carles
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5092154/
https://ncbi.nlm.nih.gov/pubmed/27253448
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2016.04.039
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