Role of the dopamine D5 receptor (DRD5) as a susceptibility gene for cervical dystonia.
Ontology highlight
ABSTRACT: Cervical dystonia (CD) is one of the most common forms of primary dystonia. The pathogenesis of the disease is still unknown, although evidence suggests a role for genetic factors. Recently, a polymorphism in the dopamine D5 receptor (DRD5) gene has been associated with the disease in a British population, suggesting that DRD5 is a susceptibility gene for CD. To confirm these data, we performed a case-control study of the microsatellite (CT/GT/GA)(n) at the DRD5 locus in 104 Italian CD patients and 104 healthy controls. The frequency of allele 4 was higher in the CD patients compared to the controls. This resulted in a twofold increased risk of developing the disease. These results provide further evidence of an association between DRD5 and cervical dystonia, supporting the involvement of
SUBMITTER: Brancati F
PROVIDER: S-EPMC1738453 | biostudies-literature | 2003 May
REPOSITORIES: biostudies-literature
ACCESS DATA