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Article

Normal dopaminergic nigrostriatal innervation in SPG3A hereditary spastic paraplegia.

Journal of neurogenetics - 1 Jan 2008

Albin Roger L, Koeppe Robert A, Rainier Shirley, Fink John K

Abstract excerpt

SPG3A/atlastin-1 gene mutations cause an autosomal dominant form of hereditary spastic paraplegia (SPG3A-HSP). We used positron emission tomography with [(11)C]DTBZ to assess nigrostriatal dopaminergic integrity in two unrelated adults with SPG3A-HSP due to the common SPG3A/atlastin-1 mutation, R...

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Identifiers

PMID: 19085270
DOI: 10.1080/01677060802337307
PMCID: PMC2743137

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19085270-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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