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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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Detalhes bibliográficos
Main Authors: Chen, Shenghan, Ondo, William G., Rao, Shaoqi, Li, Lin, Chen, Qiuyun, Wang, Qing
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2004
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1181982/
https://ncbi.nlm.nih.gov/pubmed/15077200
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