Analysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritance

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dc.contributor.authorKesim, B.
dc.contributor.authorBuyukozturk, S.
dc.contributor.authorGelincik, A.
dc.contributor.authorEraslan, S.
dc.contributor.authorUzumcu, A.
dc.contributor.authorMete, N.
dc.contributor.authorSin, A.
dc.contributor.authorOzseker, F.
dc.contributor.authorErdenen, F.
dc.contributor.authorColakoglu, B.
dc.contributor.authorDal, M.
dc.contributor.authorUyguner, O.
dc.date.accessioned2019-10-27T19:56:02Z
dc.date.available2019-10-27T19:56:02Z
dc.date.issued2008
dc.departmentEge Üniversitesien_US
dc.description27th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology -- JUN 07-11, 2008 -- Barcelona, SPAINen_US
dc.description.sponsorshipEuropean Acad Allergol & Clinical Immunolen_US
dc.identifier.endpage340en_US
dc.identifier.issn0105-4538
dc.identifier.startpage340en_US
dc.identifier.urihttps://hdl.handle.net/11454/40766
dc.identifier.volume63en_US
dc.identifier.wosWOS:000256235600906en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherBlackwell Publishingen_US
dc.relation.ispartofAllergyen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleAnalysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritanceen_US
dc.typeConference Objecten_US

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