Gelişmiş Arama

Basit öğe kaydını göster

dc.contributor.authorDurmus, H.
dc.contributor.authorMatur, Zeliha
dc.contributor.authorAtmaca, M.M.
dc.contributor.authorPoda, M.
dc.contributor.authorOflazer-Serdaroglu, P.
dc.contributor.authorDeymeer, Feza
dc.contributor.authorParman, Yeşim
dc.date.accessioned2015-01-23T13:40:22Z
dc.date.available2015-01-23T13:40:22Z
dc.date.issued2014
dc.identifier.citationDurmus H, Matur Z, Atmaca MM, Poda M, Oflazer-Serdaroglu P, Deymeer F, Parman Y. Genotypic and phenotypic presentation of TTR-FAP in Turkey. European Journal of Neurology. 2014; 21(Suppl.1): 137. Joint Congress of European Neurology, Istanbul, Turkey, May 2014en_US
dc.identifier.issn1351-5101
dc.identifier.urihttps://hdl.handle.net/11446/679en_US
dc.descriptionİstanbul Bilim Üniversitesi, Tıp Fakültesi.en_US
dc.description.abstractTransthyretin-related familial amyloid polyneuropathy (TTR-FAP) is an autosomal dominant disorder caused by mutations of the transthyretin (TTR) gene. More than 100 different mutations of the transthyretin gene were identified worlwide, but still the first described Val30Met is the most common one.en_US
dc.description.urihttp://onlinelibrary.wiley.com/doi/10.1111/ene.12495/pdfen_US
dc.language.isoengen_US
dc.publisherWiley-Blackwellen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleGenotypic and phenotypic presentation of TTR-FAP in Turkeyen_US
dc.typeconferenceObjecten_US
dc.relation.journalEuropean Journal of Neurologyen_US
dc.departmentDBÜ, Tıp Fakültesien_US
dc.identifier.issueSuppl. 1
dc.identifier.volume21
dc.identifier.startpage137
dc.identifier.endpage137
dc.contributor.authorIDTR118245en_US
dc.contributor.authorIDTR125998en_US
dc.contributor.authorIDTR126265en_US
dc.contributor.authorIDTR126263en_US
dc.contributor.authorIDTR126261en_US
dc.relation.publicationcategoryBelirsizen_US


Bu öğenin dosyaları:

Thumbnail

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster