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Article

Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals.

Journal of neurology - 1 Jan 2001

Kuhlenbäumer G, Kress W, Ringelstein E B, Stögbauer F

Abstract excerpt

X-linked recessive spinobulbar muscular atrophy (SBMA) is an adult-onset X-linked neurodegenerative disease, characterised by muscular atrophy, bulbar symptoms and endocrinological disturbances. SBMA is caused by the expansion of a CAG repeat in the androgen receptor gene. The maximum number of C...

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PMID: 11266016
DOI: 10.1007/s004150170265

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-11266016-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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