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Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?

Psychiatric genetics - 1 Dec 2001

Savić D, Topisirović I, Keckarević M, Keckarević D, Major T, Culjković B, Stojković O, Rakocević-Stojanović V, Mladenović J, Todorović S, Apostolski S, Romac S

Abstract excerpt

A number of human hereditary neuromuscular and neurodegenerative disorders are caused by the expansion of trinucleotide repeats within certain genes. The molecular mechanisms that underlie these expansions are not yet known. We have analyzed six trinucleotide repeat-containing loci [spinocerebellar ataxias (SCA1, SCA3, SCA8), dentatorubral-pallidoluysian atrophy (DRPLA), Huntington chorea (HD) and fragile X...

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PMID: 11807410
DOI: 10.1097/00041444-200112000-00004

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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