Case–Control and Family‐Based Association Study of Specific PTPRD Variants in Restless Legs Syndrome

BACKGROUND: The exact genetic causes within each of the known restless legs syndrome (RLS) loci are still unknown. Recently, it was suggested that an intronic protein tyrosine phosphatase, receptor type δ (PTPRD) single‐nucleotide polymorphism (SNP) (reference SNP no. rs2381970) is associated with i...

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Dettagli Bibliografici
Pubblicato in:Mov Disord Clin Pract
Autori principali: Gan‐Or, Ziv, Zhou, Sirui, Johnson, Amelie, Montplaisir, Jacques Y., Allen, Richard P., Earley, Christopher J., Desautels, Alex, Dion, Patrick A., Xiong, Lan, Rouleau, Guy A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2016
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Research Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6178739/
https://ncbi.nlm.nih.gov/pubmed/30363591
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.12306
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