Late-onset Huntington’s disease associated with CAG repeat lengths of 30 and 31
Author:
Funder
Medical Research Council
Wellcome Trust
National Institute for Health Research
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-021-10633-3.pdf
Reference12 articles.
1. Anil M, Mason SL, Barker RA (2020) The clinical features and progression of late-onset versus younger-onset in an adult cohort of Huntington’s disease patients. J Huntingtons Dis 9(3):275–282. https://doi.org/10.3233/JHD-200404
2. Sequeiros J, Ramos EM, Cerqueira J, Costa MC, Sousa A, Pinto-Basto J, Alonso I (2010) Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the population. Clin Genet 78(4):381–387. https://doi.org/10.1111/j.1399-0004.2010.01388.x
3. Savitt D, Jankovic J (2019) Clinical phenotype in carriers of intermediate alleles in the huntingtin gene. J Neurol Sci 402:57–61. https://doi.org/10.1016/j.jns.2019.05.010
4. Groen JL, de Bie RM, Foncke EM, Roos RA, Leenders KL, Tijssen MA (2010) Late-onset Huntington disease with intermediate CAG repeats: true or false? J Neurol Neurosurg Psychiatry 81(2):228–230. https://doi.org/10.1136/jnnp.2008.170902
5. Herishanu YO, Parvari R, Pollack Y, Shelef I, Marom B, Martino T, Cannella M, Squitieri F (2009) Huntington disease in subjects from an Israeli Karaite community carrying alleles of intermediate and expanded CAG repeats in the HTT gene: Huntington disease or phenocopy? J Neurol Sci 277(1–2):143–146. https://doi.org/10.1016/j.jns.2008.11.005
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