FUS mutations in sporadic amyotrophic lateral sclerosis

Mutations in the FUS gene have recently been described as a cause of familial ALS, but their role in the pathogenesis of sporadic ALS is unclear. We undertook mutational screening of all coding exons of FUS in 228 sporadic ALS cases, and, as previous reports suggest that exon 15 represents a mutatio...

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Bibliografiske detaljer
Main Authors: Lai, Shiao-Lin, Abramzon, Yevgeniya, Schymick, Jennifer C., Stephan, Dietrich A., Dunckley, Travis, Dillman, Allissa, Cookson, Mark, Calvo, Andrea, Battistini, Stefania, Giannini, Fabio, Caponnetto, Claudia, Mancardi, Giovanni Luigi, Spataro, Rossella, Monsurro, Maria Rosaria, Tedeschi, Gioacchino, Marinou, Kalliopi, Sabatelli, Mario, Conte, Amelia, Mandrioli, Jessica, Sola, Patrizia, Salvi, Fabrizio, Bartolomei, Ilaria, Lombardo, Federica, Mora, Gabriele, Restagno, Gabriella, Chiò, Adriano, Traynor, Bryan J.
Format: Artigo
Sprog:Inglês
Udgivet: 2010
Fag:
Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2891336/
https://ncbi.nlm.nih.gov/pubmed/20138404
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2009.12.020
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