Family-based association study of the restless legs syndrome loci 2 and 3 in a European population.

doi:10.1002/mds.21254

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Family-based association study of the restless legs syndrome loci 2 and 3 in a European population.

Movement disorders : official journal of the Movement Disorder Society - 15 Jan 2007

Kemlink David, Polo Olli, Montagna Pasquale, Provini Federica, Stiasny-Kolster Karin, Oertel Wolfgang, de Weerd Al, Nevsimalova Sona, Sonka Karel, Högl Birgit, Frauscher Birgit, Poewe Werner, Trenkwalder Claudia, Pramstaller Peter P, Ferini-Strambi Luigi, Zucconi Marco, Konofal Eric, Arnulf Isabelle, Hadjigeorgiou Georgios M, Happe Svenja, Klein Christine, Hiller Anja, Lichtner Peter, Meitinger Thomas, Müller-Myshok Betram, Winkelmann Juliane

Abstract excerpt

Three loci for the restless legs syndrome (RLS) on chromosomes 12q, 14q, and 9p (RLS1, RLS2, and RLS3) have been mapped, but no gene has been identified as yet. RLS1 has been confirmed in families from three different populations. We conducted a family-based association study of 159 European RLS trios. The subjects were genotyped using microsatellite markers evenly covering the candidate regions on chromosomes...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosomes, Human, Pair 12

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 14

Share to Chromosomes, Human, Pair 9

Share to Europe

Share to Genetic Markers

Share to International Cooperation

Share to Linkage Disequilibrium

Share to Restless Legs Syndrome

Source

Open in PubMed

Identifiers

PMID: 17133505
DOI: 10.1002/mds.21254

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Family-based association study of the restless legs syndrome loci 2 and 3 in a European population.PMID 17133505Read ↗

Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13.Semantic proximity Read ↗

Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.Semantic proximity Read ↗

Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.Semantic proximity Read ↗

Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?Semantic proximity Read ↗

[Advances in genetics of restless legs syndrome].Semantic proximity Read ↗

Restless legs syndrome: an update on genetics and future perspectives.Semantic proximity Read ↗

A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree.Semantic proximity Read ↗

A novel locus for restless legs syndrome on chromosome 13q.Semantic proximity Read ↗

Genetics of restless legs syndrome (RLS): State-of-the-art and future directions.Semantic proximity Read ↗

Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindred.Semantic proximity Read ↗

Family-based and population-based association studies validate PTPRD as a risk factor for restless legs syndrome.Semantic proximity Read ↗

RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.