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

from Section 4 - Chorea

Published online by Cambridge University Press:  04 July 2017

Kailash P. Bhatia ,
Roberto Erro  and
Maria Stamelou
By
Davina J. Hensman Moss  and
Sarah J. Tabrizi
Kailash P. Bhatia
Affiliation:
Institute of Neurology, University College London
Roberto Erro
Affiliation:
Università degli Studi di Salerno, Italy
Maria Stamelou
Affiliation:
University of Athens, Greece
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Case Studies in Movement Disorders
Common and Uncommon Presentations
 , pp. 87 - 88
Publisher: Cambridge University Press
Print publication year: 2017

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References

Suggested Readings

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.CrossRefGoogle ScholarPubMed
Rohrer, JD, Isaacs, AM, Mizielinska, S, et al. C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis. Lancet Neurol. 2015;14:291–301.Google Scholar
Wild, EJ, Tabrizi, SJ. Huntington’s disease phenocopy syndromes. Curr Opin Neurol. 2007;20:681–7.Google Scholar

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