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Advanced filters: Author: "Ian Blair" Clear advanced filters
  • Ian Blair and colleagues use genome-wide linkage analysis and whole exome sequencing to identify mutations in the CCNF gene in large cohorts of amyotrophic lateral sclerosis and frontotemporal dementia patients. In addition to validating the mutations in international cohorts, the authors also show that mutant CCNFgene product affects ubiquitination and protein degradation in cultured cells.

    • Kelly L. Williams
    • Simon Topp
    • Ian P. Blair
    ResearchOpen Access
    Nature Communications
    Volume: 7, P: 1-8