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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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| Veröffentlicht in: | BMJ Neurol Open |
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| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Publishing Group
2020
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| Schlagworte: | |
| Online Zugang: | 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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