MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels

Restless legs syndrome (RLS) is a common neurological disorder characterized by an irresistible urge to move the legs at night, which is often accompanied by unpleasant sensations. A recent genomewide association study identified an association between RLS and intronic markers from the MEIS1 gene. C...

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Detalhes bibliográficos
Main Authors: Xiong, Lan, Catoire, Hélène, Dion, Patrick, Gaspar, Claudia, Lafrenière, Ronald G., Girard, Simon L., Levchenko, Anastasia, Rivière, Jean-Baptiste, Fiori, Laura, St-Onge, Judith, Bachand, Isabelle, Thibodeau, Pascale, Allen, Richard, Earley, Christopher, Turecki, Gustavo, Montplaisir, Jacques, Rouleau, Guy A.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2009
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2722232/
https://ncbi.nlm.nih.gov/pubmed/19126776
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn443
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