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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

dc.contributor.authorOzseker, F.
dc.contributor.authorGelincik, A.
dc.contributor.authorColakoglu, B.
dc.contributor.authorDal, M.
dc.contributor.authorUyguner, O.
dc.contributor.authorKesim, B.
dc.contributor.authorBuyukozturk, S.
dc.contributor.authorEraslan, S.
dc.contributor.authorUzumcu, A.
dc.contributor.authorMete, N.
dc.contributor.authorSin, A.
dc.contributor.authorErdenen, F.
dc.date.accessioned2021-03-04T09:04:04Z
dc.date.available2021-03-04T09:04:04Z
dc.identifier.citationKesim B., Buyukozturk S., Gelincik A., Eraslan S., Uzumcu A., Mete N., Sin A., Ozseker F., Erdenen F., Colakoglu B., et al., "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", 27th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology, Barcelona, İspanya, 7 - 11 Haziran 2008, cilt.63, ss.340
dc.identifier.othervv_1032021
dc.identifier.otherav_6682f73d-282d-41e4-8cea-374527918ee7
dc.identifier.urihttp://hdl.handle.net/20.500.12627/71180
dc.language.isoeng
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectKlinik Tıp (MED)
dc.subjectİmmünoloji
dc.subjectKlinik Tıp
dc.subjectALERJİ
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 inheritance
dc.typeBildiri
dc.contributor.departmentDuzen Laboratory Group , ,
dc.identifier.volume63
dc.contributor.firstauthorID134605


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