What do we know about Late Onset Huntington’s Disease?-Reference-Cited by-同舟云学术

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What do we know about Late Onset Huntington’s Disease?

Published:2017-06-30 Issue:2 Volume:6 Page:95-103
ISSN:1879-6397
Container-title:Journal of Huntington's Disease
language:
Short-container-title:JHD

Author:

Chaganti Sai S.¹²,McCusker Elizabeth A.¹²,Loy Clement T.¹³⁴

Affiliation:

1. Huntington Disease Service, Westmead Hospital, Sydney, Australia

2. Sydney Medical School, The University of Sydney, Sydney, Australia

3. School of Public Health, The University of Sydney, Sydney, Australia

4. The Garvan Institute of Medical Research, Sydney, Australia

Publisher

IOS Press

Subject

Cellular and Molecular Neuroscience,Clinical Neurology

Reference60 articles.

1. The Huntington’s Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. Cell. 1993;72(6):971–83.

2. The HTT CAG-expansion mutation determines age at death but not disease duration in Huntington disease;Keum;Am J Hum Genet,2016

3. Late onset of Huntington’s disease;Myers;J Neurol Neurosurg Psychiatry,1985

4. Differences in duration of Huntington’s disease based on age at onset;Foroud;J Neurol Neurosurg Psychiatry,1999

5. Severity of cognitive impairment in juvenile and late-onset Huntington disease;Gómez-Tortosa;Arch Neurol,1998

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