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COMPLEMENT FACTOR H MUTATION IN C3 GLOMERULOPATHY WITH INITIAL PRESENTATION AS HEMOLYTIC UREMIC SYNDROME: A CASE REPORT

dc.contributor.authorCicek, Neslihan
dc.contributor.authorYILDIZ, NURDAN
dc.contributor.authorGÖKCE, İBRAHİM
dc.contributor.authorSAK, MEHTAP
dc.contributor.authorKilicaslan, Isin
dc.contributor.authorALPAY, HARİKA
dc.date.accessioned2021-03-06T11:28:46Z
dc.date.available2021-03-06T11:28:46Z
dc.date.issued2018
dc.identifier.citationYILDIZ N., SAK M., Kilicaslan I., Cicek N., GÖKCE İ., ALPAY H., "COMPLEMENT FACTOR H MUTATION IN C3 GLOMERULOPATHY WITH INITIAL PRESENTATION AS HEMOLYTIC UREMIC SYNDROME: A CASE REPORT", PEDIATRIC NEPHROLOGY, cilt.33, ss.1906-1907, 2018
dc.identifier.issn0931-041X
dc.identifier.othervv_1032021
dc.identifier.otherav_ef42a487-e171-4fd0-b166-83f0a2e837fa
dc.identifier.urihttp://hdl.handle.net/20.500.12627/157030
dc.language.isoeng
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectNefroloji
dc.subjectİç Hastalıkları
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.titleCOMPLEMENT FACTOR H MUTATION IN C3 GLOMERULOPATHY WITH INITIAL PRESENTATION AS HEMOLYTIC UREMIC SYNDROME: A CASE REPORT
dc.typeMakale
dc.relation.journalPEDIATRIC NEPHROLOGY
dc.contributor.departmentMarmara Üniversitesi , Tıp Fakültesi , Çocuk Sağlığı Ve Hastalıkları Anabilim Dalı
dc.identifier.volume33
dc.identifier.issue10
dc.identifier.startpage1906
dc.identifier.endpage1907
dc.contributor.firstauthorID256947


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