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[To date, RAN translation has been implicated in 4 nucleotide repeat expansion disorders: spinocerebellar ataxia type 8; myotonic dystrophy type 1 with CTG�CAG repeats; C9orf72 amyotrophic lateral sclerosis/frontotemporal dementia with GGGGCC�GGCCCC repeats; and fragile X-associated tremor/ataxia syndrome with CGG repeats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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