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BZRAP1 (RIM-BP1) mutations cause a novel autosomal recessive dystonia syndrome

dc.contributor.authorPak, M.
dc.contributor.authorPajusalu, S.
dc.contributor.authorMencacci, N. E.
dc.contributor.authorAtasu, B.
dc.contributor.authorRein, R.
dc.contributor.authorPuusepp, S.
dc.contributor.authorReinson, K.
dc.contributor.authorTomberg, T.
dc.contributor.authorWiethoff, S.
dc.contributor.authorPapandreou, A.
dc.contributor.authorWarner, T. T.
dc.contributor.authorBalint, B.
dc.contributor.authorBhatia, K. P.
dc.contributor.authorGasser, T.
dc.contributor.authorSimon-Sanchez, J.
dc.contributor.authorKurian, M. A.
dc.contributor.authorAcuna, C.
dc.contributor.authorLohmann, E.
dc.contributor.authorWood, N.
dc.contributor.authorOunap, K.
dc.date.accessioned2021-03-03T15:01:16Z
dc.date.available2021-03-03T15:01:16Z
dc.identifier.citationPajusalu S., Mencacci N. E. , Atasu B., Rein R., Puusepp S., Reinson K., Tomberg T., Wiethoff S., Papandreou A., Warner T. T. , et al., "BZRAP1 (RIM-BP1) mutations cause a novel autosomal recessive dystonia syndrome", 50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.41
dc.identifier.otherav_3cbdf393-7777-4228-bf23-a8d09fba54d4
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/44747
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectSitogenetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.titleBZRAP1 (RIM-BP1) mutations cause a novel autosomal recessive dystonia syndrome
dc.typeBildiri
dc.contributor.departmentTartu Univ Hosp , ,
dc.identifier.volume26
dc.contributor.firstauthorID154930


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