Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort

OBJECTIVE: Mutations in the FUS gene on chromosome 16 have been recently discovered as a cause of familial amyotrophic lateral sclerosis (FALS). This study determined the frequency and identities of FUS gene mutations in a cohort of Italian patients with FALS. METHODS: We screened all 15 coding exon...

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Hoofdauteurs: Ticozzi, N, Silani, V, LeClerc, A L., Keagle, P, Gellera, C, Ratti, A, Taroni, F, Kwiatkowski, T J., McKenna-Yasek, D M., Sapp, P C., Brown, R H., Landers, J E.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Academy of Neurology 2009
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Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2764725/
https://ncbi.nlm.nih.gov/pubmed/19741215
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e3181bbff05
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