Biomarkers for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Associated With Hexanucleotide Expansion Mutations in C9orf72
Author:
Funder
National Institutes of Health
Muscular Dystrophy Association
Target ALS
Publisher
Frontiers Media SA
Subject
Neurology (clinical),Neurology
Reference85 articles.
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2. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD;Renton;Neuron,2011
3. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS;DeJesus-Hernandez;Neuron,2011
4. C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis;Rohrer;Lancet Neurol.,2015
5. Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72;Murray;Acta Neuropathol,2011
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