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- W1979402493 abstract "The C9orf72 expansion mutation was identified in 10 of 514 patients (1.95%) with Huntington disease (HD) phenocopy presentations. This suggests that neurologists should consider and test for C9orf72 expansions in those with HD-like disorders, and, more broadly, demonstrates that C9orf72 has a more extensive phenotype than previously identified, including movement disorders." @default.
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- W1979402493 date "2014-01-27" @default.
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- W1979402493 title "Spotlight on the January 28 Issue" @default.
- W1979402493 doi "https://doi.org/10.1212/wnl.0000000000000059" @default.
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