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Rapidly Progressive Dementia in a Chinese Patient due to C9ORF72 Mutation

Published online by Cambridge University Press:  02 December 2014

Nagaendran Kandiah
Affiliation:
National Neuroscience Institute, Singapore
Pheth Sengdy
Affiliation:
University of British Columbia, Vancouver, BC, Canada Email: hsiung@mail.ubc.ca
Ian R. A. Mackenzie
Affiliation:
University of British Columbia, Vancouver, BC, Canada Email: hsiung@mail.ubc.ca
Ging-Yuek R. Hsiung
Affiliation:
University of British Columbia, Vancouver, BC, Canada Email: hsiung@mail.ubc.ca
Mariely DeJesus-Hernandez
Affiliation:
Mayo Clinic Jacksonville, Jacksonville, Florida, USA
Rosa Rademakers
Affiliation:
Mayo Clinic Jacksonville, Jacksonville, Florida, USA
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Abstract

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Type
Letters to the Editor
Copyright
Copyright © The Canadian Journal of Neurological 2012

References

1.DeJesus-Hernandez, M, Mackenzie, IR, Boeve, BF, et al.Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron. 2011;72(2):24556.CrossRefGoogle Scholar
2.Hodges, J.Familial frontotemporal dementia and amyotrophic lateral sclerosis associated with the C9ORF72 hexanucleotide repeat. Brain. 2012;135:6525.CrossRefGoogle Scholar
3.Mok, K, Traynor, BJ, Schymick, J, et al.The chromosome 9 ALS and FTD locus is probably derived from a single founder. Neurobiol Aging. 2012;33(1):209 e38.CrossRefGoogle Scholar
4.Hou, CE, Yaffe, K, Perez-Stable, EJ, Miller, BL.Frequency of dementia etiologies in four ethnic groups. Dement Geriatr Cogn Disord. 2006; 22(1): 427.CrossRefGoogle Scholar
5.Cronin, S, Hardiman, O, Traynor, BJ.Ethnic variation in the incidence of ALS: a systematic review. Neurology. 2007; 68(13): 10027.CrossRefGoogle ScholarPubMed
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