| pubmed-article:16966564 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16966564 | lifeskim:mentions | umls-concept:C0008633 | lld:lifeskim |
| pubmed-article:16966564 | lifeskim:mentions | umls-concept:C1708726 | lld:lifeskim |
| pubmed-article:16966564 | lifeskim:mentions | umls-concept:C1521045 | lld:lifeskim |
| pubmed-article:16966564 | lifeskim:mentions | umls-concept:C2931830 | lld:lifeskim |
| pubmed-article:16966564 | lifeskim:mentions | umls-concept:C0024779 | lld:lifeskim |
| pubmed-article:16966564 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:16966564 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:16966564 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:16966564 | pubmed:dateCreated | 2006-9-12 | lld:pubmed |
| pubmed-article:16966564 | pubmed:abstractText | The authors investigated genetic factors contributing to restless legs syndrome (RLS) by performing a 10-cM genome-wide scan in a large French-Canadian pedigree. They detected an autosomal-dominant locus mapping to chromosome 20p13, with a maximum multipoint lod score of 3.86 at marker D20S849. This is the third reported autosomal-dominant locus for RLS and the first autosomal-dominant RLS locus in the French-Canadian population. | lld:pubmed |
| pubmed-article:16966564 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16966564 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16966564 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:16966564 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16966564 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:16966564 | pubmed:issn | 1526-632X | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:MontplaisirJ... | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:RouleauG AGA | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:XiongLL | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:DubéM PMP | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:ProvostSS | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:TureckiGG | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:LevchenkoAA | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:DesautelsAA | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:St-OngeJJ | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:ThibodeauPP | lld:pubmed |
| pubmed-article:16966564 | pubmed:author | pubmed-author:RivièreJ BJB | lld:pubmed |
| pubmed-article:16966564 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:16966564 | pubmed:day | 12 | lld:pubmed |
| pubmed-article:16966564 | pubmed:volume | 67 | lld:pubmed |
| pubmed-article:16966564 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16966564 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16966564 | pubmed:pagination | 900-1 | lld:pubmed |
| pubmed-article:16966564 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:meshHeading | pubmed-meshheading:16966564... | lld:pubmed |
| pubmed-article:16966564 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16966564 | pubmed:articleTitle | A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13. | lld:pubmed |
| pubmed-article:16966564 | pubmed:affiliation | Center for the Study of Brain Diseases, CHUM Research Center-Notre Dame Hospital, Montreal, Quebec, Canada. | lld:pubmed |
| pubmed-article:16966564 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16966564 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:16966564 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16966564 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16966564 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16966564 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16966564 | lld:pubmed |
