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Article

Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patients.

Neuroscience letters - 21 Jun 2018

Mongelli Alessia, Sarro Lidia, Rizzo Elena, Nanetti Lorenzo, Meucci Nicoletta, Pezzoli Gianni, Goldwurm Stefano, Taroni Franco, Mariotti Caterina, Gellera Cinzia

Abstract excerpt

Multiple system atrophy (MSA) is an adult onset, progressive, neurodegenerative disorder of unknown etiology characterized by autonomic dysfunction, parkinsonism (MSA-P) and cerebellar ataxia (MSA-C). The phenotypic spectrum may present overlapping features with other neurodegenerative diseases, particularly the autosomal dominant inherited polyglutamine disorders. To investigate the possible contribution of CAG...

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PMID: 29715545
DOI: 10.1016/j.neulet.2018.04.044

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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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