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Article

Proteomic Analysis of Huntington's Disease.

Current protein & peptide science - 1 Jan 2020

Kumar Shobhit, Singh Priyanka, Sharma Shrestha, Ali Javed, Baboota Sanjula, Pottoo Faheem Hyder

Abstract excerpt

Huntington's disease (HD) is a neurodegenerative disease that is genetically inherited through an autosomal dominant gene located on chromosome 4. HD is caused by DNA mutation (generally 37 or more repetition of CAG nucleotides) that leads to an excessive stretch of glutamine residues. However, the main pathogenesis pathway resulted by polyglutamine expansion in mutant HD is unknown. The characteristics of this...

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Identifiers

PMID: 33023443
DOI: 10.2174/1389203721666201006160327

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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