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

Simple item page
dc.contributor.authorsYildiz, Nurdan; Sak, Mehtap; Kilicaslan, Isin; Cicek, Neslihan; Gokce, Ibrahim; Alpay, Harika
dc.date.accessioned2022-03-10T17:57:38Z
dc.date.accessioned2026-01-11T07:17:10Z
dc.date.available2022-03-10T17:57:38Z
dc.date.issued2018
dc.identifier.doidoiWOS:000443998400321
dc.identifier.eissn1432-198X
dc.identifier.issn0931-041X
dc.identifier.urihttps://hdl.handle.net/11424/222091
dc.identifier.wosWOS:000443998400321
dc.language.isoeng
dc.publisherSPRINGER
dc.relation.ispartofPEDIATRIC NEPHROLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleCOMPLEMENT FACTOR H MUTATION IN C3 GLOMERULOPATHY WITH INITIAL PRESENTATION AS HEMOLYTIC UREMIC SYNDROME: A CASE REPORT
dc.typeconferenceObject
dc.type.submeetingabstract
dspace.entity.typePublication
oaire.citation.endPage1907
oaire.citation.issue10
oaire.citation.startPage1906
oaire.citation.titlePEDIATRIC NEPHROLOGY
oaire.citation.volume33

Files

Collections

Araştırma Çıktıları