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Article

DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystonia.

Parkinsonism & related disorders - 1 Jul 2014

Groen Justus L, Ritz Katja, Warner Tom T, Baas Frank, Tijssen Marina A J

Abstract excerpt

The dystonias are a clinical heterogeneous group with a complex genetic background. To gain more insight in genetic risk factors in dystonia we used a pathway sequence approach in patients with an extreme dystonia phenotype (n = 26). We assessed all coding and non-coding variants in candidate gen...

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Source

Identifiers

PMID: 24768614
DOI: 10.1016/j.parkreldis.2014.04.002

Genes

DRD1
THAP1
DRD5
KLC1
SNAPIN
STON2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24768614-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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