Article ID Journal Published Year Pages File Type
8285539 Parkinsonism & Related Disorders 2018 6 Pages PDF
Abstract
Carriers of DRD2 risk haplotypes and possibly the BDNF variants rs6265 and DRD3 haplotypes, were at increased risk of dyskinesia, suggesting that these genes may be involved in dyskinesia related pathomechanisms. PD patients with these genetic variants might be prime candidates for treatments aiming to prevent or delay the onset of dyskinesia.
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Life Sciences Biochemistry, Genetics and Molecular Biology Ageing
Authors
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