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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Foilsithe in: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
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2016
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Article
Rochtain Ar Líne: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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