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Exome sequencing in a family with restless legs syndrome

dc.contributor.authorStephani, Ulrich
dc.contributor.authorLohmann, Katja
dc.contributor.authorHagenah, Johann
dc.contributor.authorPramstaller, Peter P.
dc.contributor.authorKlein, Christine
dc.contributor.authorMuhle, Hiltrud
dc.contributor.authorPichler, Irene
dc.contributor.authorWeissbach, Anne
dc.contributor.authorSiegesmund, Katharina
dc.contributor.authorBrueggemann, Norbert
dc.contributor.authorKasten, Meike
dc.contributor.authorSchmidt, Alexander
dc.contributor.authorLohmann, Ebba
dc.contributor.authorLohnau, Thora
dc.contributor.authorSchwinger, Eberhard
dc.date.accessioned2021-03-03T18:55:58Z
dc.date.available2021-03-03T18:55:58Z
dc.date.issued2012
dc.identifier.citationWeissbach A., Siegesmund K., Brueggemann N., Schmidt A., Kasten M., Pichler I., Muhle H., Lohmann E., Lohnau T., Schwinger E., et al., "Exome sequencing in a family with restless legs syndrome", MOVEMENT DISORDERS, cilt.27, sa.13, ss.1686-1689, 2012
dc.identifier.issn0885-3185
dc.identifier.othervv_1032021
dc.identifier.otherav_51cf9e04-7726-4302-955d-9c47d537cd03
dc.identifier.urihttp://hdl.handle.net/20.500.12627/58131
dc.identifier.urihttps://doi.org/10.1002/mds.25191
dc.description.abstractBackground: Restless legs syndrome (RLS) has a high familial aggregation. To date, several loci and genetic risk factors have been identified, but no causative gene mutation has been found.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleExome sequencing in a family with restless legs syndrome
dc.typeMakale
dc.relation.journalMOVEMENT DISORDERS
dc.contributor.departmentUniversity of Kiel , ,
dc.identifier.volume27
dc.identifier.issue13
dc.identifier.startpage1686
dc.identifier.endpage1689
dc.contributor.firstauthorID206856


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