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Genomewide Linkage Scan Identifies a Novel Susceptibility Locus for Restless Legs Syndrome on Chromosome 9p

Restless legs syndrome (RLS) is a common neurological disorder that affects 5%–12% of all whites. To genetically dissect this complex disease, we characterized 15 large and extended multiplex pedigrees, consisting of 453 subjects (134 affected with RLS). A familial aggregation analysis was performed...

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Bibliographische Detailangaben
Hauptverfasser: Chen, Shenghan, Ondo, William G., Rao, Shaoqi, Li, Lin, Chen, Qiuyun, Wang, Qing
Format: Artigo
Sprache:Inglês
Veröffentlicht: The American Society of Human Genetics 2004
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Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1181982/
https://ncbi.nlm.nih.gov/pubmed/15077200
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