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Genetics of restless legs syndrome (RLS): State-of-the-art and future directions

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Autor
Winkelmann, J.; Polo, O.; Provini, F.; Nevsimalova, S.; Kemlink, D.; Sonka, K.; Hogl, B.; Poewe, W.; Stiasny-Kolster, K.; Oertel, W.; de Weerd, A.; Strambi, L. F.; Zucconi, M.; Pramstaller, P. P.; Arnulf, I.; Trenkwalder, C.; Klein, C.; Hadjigeorgiou, G. M.; Happe, S.; Rye, D.; Montagna, P.
Fecha
2007
DOI
10.1002/mds.21587
Materia
restless legs syndrome
genetics
steep
TYROLEAN POPULATION ISOLATE
RISK-FACTORS
SUSCEPTIBILITY LOCUS
SEGREGATION ANALYSIS
CHROMOSOME 9P
ASSOCIATION
LINKAGE
FAMILY
SLEEP
PREVALENCE
Clinical Neurology
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Resumen
Several 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.
URI
http://hdl.handle.net/11615/34678
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]
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