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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Bibliografski detalji
Izdano u:Neuron
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: 2016
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Article
Online pristup: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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