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Novel FUS mutation in patients with sporadic amyotrophic lateral sclerosis and corticobasal degeneration

โœ Scribed by Nagayama, Shigemi; Minato-Hashiba, Naomi; Nakata, Michiyo; Kaito, Muichi; Nakanishi, Megumi; Tanaka, Keiko; Arai, Makoto; Akiyama, Haruhiko; Matsui, Makoto


Book ID
119305193
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
256 KB
Volume
19
Category
Article
ISSN
0967-5868

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De novo truncating FUS gene mutation as
โœ Mariely DeJesus-Hernandez; Jannet Kocerha; NiCole Finch; Richard Crook; Matt Bak ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 441 KB ๐Ÿ‘ 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