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Article

ETS1 regulates the expression of ATXN2.

Human molecular genetics - 1 Dec 2012

Scoles Daniel R, Pflieger Lance T, Thai Khanh K, Hansen Stephen T, Dansithong Warunee, Pulst Stefan-M

Abstract excerpt

Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant disorder caused by the expansion of a CAG tract in the ATXN2 gene. The SCA2 phenotype is characterized by cerebellar ataxia, neuropathy and slow saccades. SCA2 foreshortens life span and is currently without symptomatic or disease-modi...

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Source

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Identifiers

PMID: 22914732
DOI: 10.1093/hmg/dds349
PMCID: PMC3490512

Genes

ATXN2
ETS1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22914732-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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