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Article

Linkage with the Ser9Gly DRD3 polymorphism in essential tremor families

27 Apr 2006

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16650084
DOI: 10.1111/j.1399-0004.2006.00600.x

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Linkage with the Ser9Gly DRD3 polymorphism in essential tremor familiesPMID 16650084Read ↗

DRD3 variant and risk of essential tremor.Semantic proximity Read ↗

Reappraisal of the role of the DRD3 gene in essential tremor.Semantic proximity Read ↗

DRD3 Ser9Gly variant is not associated with essential tremor in a series of Italian patients.Semantic proximity Read ↗

Meta-analysis of the influence of DRD3 Ser9Gly variant on susceptibility for essential tremor.Semantic proximity Read ↗

Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients.Semantic proximity Read ↗

A family study of DRD3 rs6280, SLC1A2 rs3794087 and MAPT rs1052553 variants in essential tremor.Semantic proximity Read ↗

A functional variant of the dopamine D3 receptor is associated with risk and age-at-onset of essential tremor.Semantic proximity Read ↗

Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?Semantic proximity Read ↗

Case-control study of patients with essential tremor in Latvia.Semantic proximity Read ↗

DRD3 Ser9Gly and HS1BP3 Ala265Gly are not associated with Parkinson disease.Semantic proximity Read ↗

Dinucleotide repeat polymorphism (D3S1776) on human chromosome 3p.Semantic proximity Read ↗

[Association between polymorphisms in the human dopamine D3 receptor gene and genetic susceptibility of essential tremor].Semantic proximity Read ↗

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