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  • Print publication year: 2017
  • Online publication date: July 2017

37 - A Newly Recognized HD-Phenocopy Associated with C9orf72 Expansion

from Section 4 - Chorea
Hensman Moss, DJ, Poulter, M, Beck, J, et al. C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. Neurology. 2014;82:292–9.
Rohrer, JD, Isaacs, AM, Mizielinska, S, et al. C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis. Lancet Neurol. 2015;14:291301.
Wild, EJ, Tabrizi, SJ. Huntington’s disease phenocopy syndromes. Curr Opin Neurol. 2007;20:681–7.