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Case report and literature review of Huntington disease with intermediate CAG expansion

BACKGROUND: Huntington disease (HD) is a genetically inherited neurodegenerative disorder that classically involves a trinucleotide CAG repeat expansion on chromosome 4, with 36 repeats or greater being disease identifying. It generally presents between the age of 30 and 40 years old and is characte...

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Bibliografiset tiedot
Julkaisussa:BMJ Neurol Open
Päätekijät: Jevtic, Stefan D, Provias, John P
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMJ Publishing Group 2020
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7871728/
https://ncbi.nlm.nih.gov/pubmed/33681777
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjno-2019-000027
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