Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Kaffe, Maria"'
Autor:
Kaffe, Maria
During my doctoral work I investigated and identified the link between the intronic restless legs syndrome (RLS)-association signal within MEIS1 and its functional correlate. MEIS1 is a highly conserved homeobox developmental gene. Through screening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______518::093142cdf32b45cae5dfa68c7ba220c9
https://mediatum.ub.tum.de/doc/1131529/document.pdf
https://mediatum.ub.tum.de/doc/1131529/document.pdf
Autor:
Schormair, Barbara, Plag, Jens, Kaffe, Maria, Gross, Nadine, Czamara, Darina, Samtleben, Walter, Lichtner, Peter, Ströhle, Andreas, Stefanidis, Ioannis, Vainas, Andreas, Dardiotis, Efthimios, Sakkas, George K, Müller-Mhysok, Bertram, Meitinger, Thomas, Heemann, Uwe, Hadjigeorgiou, Georgios M, Oexle, Konrad, Winkelmann, Juliane, Gieger, Christian
Publikováno v:
Journal of Medical Genetics
Journal of Medical Genetics, BMJ Publishing Group, 2011, 48 (7), pp.462. ⟨10.1136/jmg.2010.087858⟩
Journal of Medical Genetics, BMJ Publishing Group, 2011, 48 (7), pp.462. ⟨10.1136/jmg.2010.087858⟩
International audience; Background: Restless legs syndrome (RLS) is a sleep-related movement disorder that occurs both in an idiopathic form and in symptomatic varieties. RLS is a frequent and distressing comorbidity in end-stage renal disease (ESRD)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::510018ca4f1fcf385a9c55c97d161f8d
https://hal.archives-ouvertes.fr/hal-00632283/document
https://hal.archives-ouvertes.fr/hal-00632283/document