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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Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2010
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Accesso online: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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