Transcriptome Study in Sicilian Patients with Huntington’s Disease
<b>Background/Objectives</b>: Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder caused by the expansion of the CAG nucleotide repeat in the first exon of the huntingtin (<i>HTT</i>) gene. The disease typically manifests between the second and third...
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| Main Authors: | , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2025-02-01
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| Series: | Diagnostics |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2075-4418/15/4/409 |
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