Title : De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis.

Pub. Date : 2010 May

PMID : 20232451






1 Functional Relationships(s)
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1 We further identified a novel in-frame insertion/deletion mutation in FUS exon 12 (p.S402_P411delinsGGGG) which is predicted to expand a conserved poly-glycine motif. polyglycine FUS RNA binding protein Homo sapiens