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FUS mutations in sporadic amyotrophic lateral sclerosis

✍ Scribed by Shiao-Lin Lai; Yevgeniya Abramzon; Jennifer C. Schymick; Dietrich A. Stephan; Travis Dunckley; Allissa Dillman; Mark Cookson; Andrea Calvo; Stefania Battistini; Fabio Giannini; Claudia Caponnetto; Giovanni Luigi Mancardi; Rossella Spataro; Maria Rosaria Monsurro; Gioacchino Tedeschi; Kalliopi Marinou; Mario Sabatelli; Amelia Conte; Jessica Mandrioli; Patrizia Sola; Fabrizio Salvi; Ilaria Bartolomei; Federica Lombardo; Gabriele Mora; Gabriella Restagno; Adriano Chiò; Bryan J. Traynor


Book ID
116781580
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
239 KB
Volume
32
Category
Article
ISSN
0197-4580

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De novo truncating FUS gene mutation as
✍ Mariely DeJesus-Hernandez; Jannet Kocerha; NiCole Finch; Richard Crook; Matt Bak 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 441 KB 👁 1 views

Mutations in the gene encoding fused in sarcoma (FUS) were recently identified as a novel cause of amyotrophic lateral sclerosis (ALS), emphasizing the genetic heterogeneity of ALS. We sequenced the genes encoding superoxide dismutase (SOD1), TAR DNA-binding protein 43 (TARDBP) and FUS in 99 sporadi