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dc.contributor.authorBrandt, Tobias
dc.contributor.authorde Freitas, Gabriel R.
dc.contributor.authorThie, Andreas
dc.contributor.authorMachetanz, Jochen
dc.contributor.authorBaumgartner, Ralf W.
dc.contributor.authorDichgans, Martin
dc.contributor.authorEngelter, Stefan T.
dc.contributor.authorSiva, Aksel
dc.contributor.authorAltintas, Ayse
dc.contributor.authorGrond-Ginsbach, Caspar
dc.contributor.authorKloss, Manja
dc.contributor.authorAksay, Suna Su
dc.contributor.authorLyrer, Philipp
dc.contributor.authorTraenka, Christopher
dc.contributor.authorErhart, Philipp
dc.contributor.authorJose Martin, Juan
dc.date.accessioned2021-03-05T20:26:12Z
dc.date.available2021-03-05T20:26:12Z
dc.date.issued2017
dc.identifier.citationGrond-Ginsbach C., Brandt T., Kloss M., Aksay S. S. , Lyrer P., Traenka C., Erhart P., Jose Martin J., Altintas A., Siva A., et al., "Next generation sequencing analysis of patients with familial cervical artery dissection", EUROPEAN STROKE JOURNAL, cilt.2, ss.137-143, 2017
dc.identifier.othervv_1032021
dc.identifier.otherav_d435b26e-2558-4c02-aa55-62315a7bd642
dc.identifier.urihttp://hdl.handle.net/20.500.12627/140058
dc.identifier.urihttps://doi.org/10.1177/2396987317693402
dc.description.abstractBackground: The cause of cervical artery dissection is not well understood. We test the hypothesis that mutations in genes associated with known arterial connective tissue disorders are enriched in patients with familial cervical artery dissection.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.titleNext generation sequencing analysis of patients with familial cervical artery dissection
dc.typeMakale
dc.relation.journalEUROPEAN STROKE JOURNAL
dc.contributor.departmentRuprecht Karls University Heidelberg , ,
dc.identifier.volume2
dc.identifier.issue2
dc.identifier.startpage137
dc.identifier.endpage143
dc.contributor.firstauthorID243439


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