Source:http://linkedlifedata.com/resource/pubmed/id/16966564
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2006-9-12
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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.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1526-632X
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
12
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pubmed:volume |
67
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
900-1
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:16966564-Chromosome Mapping,
pubmed-meshheading:16966564-Chromosomes, Human, Pair 20,
pubmed-meshheading:16966564-Family Health,
pubmed-meshheading:16966564-Female,
pubmed-meshheading:16966564-Genetic Linkage,
pubmed-meshheading:16966564-Genetic Predisposition to Disease,
pubmed-meshheading:16966564-Genotype,
pubmed-meshheading:16966564-Humans,
pubmed-meshheading:16966564-Lod Score,
pubmed-meshheading:16966564-Male,
pubmed-meshheading:16966564-Restless Legs Syndrome
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pubmed:year |
2006
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pubmed:articleTitle |
A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13.
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pubmed:affiliation |
Center for the Study of Brain Diseases, CHUM Research Center-Notre Dame Hospital, Montreal, Quebec, Canada.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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