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dc.creatorWinkelmann, J.en
dc.creatorPolo, O.en
dc.creatorProvini, F.en
dc.creatorNevsimalova, S.en
dc.creatorKemlink, D.en
dc.creatorSonka, K.en
dc.creatorHogl, B.en
dc.creatorPoewe, W.en
dc.creatorStiasny-Kolster, K.en
dc.creatorOertel, W.en
dc.creatorde Weerd, A.en
dc.creatorStrambi, L. F.en
dc.creatorZucconi, M.en
dc.creatorPramstaller, P. P.en
dc.creatorArnulf, I.en
dc.creatorTrenkwalder, C.en
dc.creatorKlein, C.en
dc.creatorHadjigeorgiou, G. M.en
dc.creatorHappe, S.en
dc.creatorRye, D.en
dc.creatorMontagna, P.en
dc.date.accessioned2015-11-23T10:54:13Z
dc.date.available2015-11-23T10:54:13Z
dc.date.issued2007
dc.identifier10.1002/mds.21587
dc.identifier.issn0885-3185
dc.identifier.urihttp://hdl.handle.net/11615/34678
dc.description.abstractSeveral studies demonstrated that 60% of restless legs syndrome (RLS) patients have a positive family history and it has been suggested that RLS is a highly hereditary trait. To date, several loci have been mapped but no gene has been identified yet. Phenocopies and possible nonpenetrants made it difficult to detect a common segregating haplotype within the families. Defining the exact candidate region is hampered by possible intrafamilial, allelic, and nonallelic heterogeneity. One important prerequisite for future successful genetic studies in RLS is the availability of large and thoroughly phenotyped patients and family samples for linkage as well as association studies. (C) 2007 Movement Disorder Society.en
dc.sourceMovement Disordersen
dc.source.uri<Go to ISI>://WOS:000251605200010
dc.subjectrestless legs syndromeen
dc.subjectgeneticsen
dc.subjectsteepen
dc.subjectTYROLEAN POPULATION ISOLATEen
dc.subjectRISK-FACTORSen
dc.subjectSUSCEPTIBILITY LOCUSen
dc.subjectSEGREGATION ANALYSISen
dc.subjectCHROMOSOME 9Pen
dc.subjectASSOCIATIONen
dc.subjectLINKAGEen
dc.subjectFAMILYen
dc.subjectSLEEPen
dc.subjectPREVALENCEen
dc.subjectClinical Neurologyen
dc.titleGenetics of restless legs syndrome (RLS): State-of-the-art and future directionsen
dc.typejournalArticleen


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