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: Michele Salemi, Vincenzo Di Stefano, Francesca A. Schillaci, Giovanna Marchese, Maria Grazia Salluzzo, Angela Cordella, Ilenia De Leo, Concetta Simona Perrotta, Giuseppe Nibali, Giuseppe Lanza, Raffaele Ferri
Format: Article
Language:English
Published: MDPI AG 2025-02-01
Series:Diagnostics
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Online Access:https://www.mdpi.com/2075-4418/15/4/409
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