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A Case Of Atypical Hemolytic Uremic Syndrome Due To Cobalamin C Disorder Caused By A New Mutation In Mmachc Gene

dc.contributor.authorCaliskan, Salim
dc.contributor.authorKiykim, Ertuğrul
dc.contributor.authorAdrovic, Amra
dc.contributor.authorSever, Lale
dc.contributor.authorBAUMGARTNER, Matthias R.
dc.contributor.authorAgbas, Ayse
dc.contributor.authorCanpolat, Nur
dc.date.accessioned2021-03-05T15:46:36Z
dc.date.available2021-03-05T15:46:36Z
dc.date.issued2014
dc.identifier.citationAdrovic A., Canpolat N., Caliskan S., Kiykim E., BAUMGARTNER M. R. , Agbas A., Sever L., "A Case Of Atypical Hemolytic Uremic Syndrome Due To Cobalamin C Disorder Caused By A New Mutation In Mmachc Gene", PEDIATRIC NEPHROLOGY, cilt.29, ss.1834, 2014
dc.identifier.issn0931-041X
dc.identifier.otherav_bd76b887-1ece-4150-bae1-c9b9c8794132
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/125897
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectTıp
dc.subjectİç Hastalıkları
dc.subjectNefroloji
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.subjectDahili Tıp Bilimleri
dc.titleA Case Of Atypical Hemolytic Uremic Syndrome Due To Cobalamin C Disorder Caused By A New Mutation In Mmachc Gene
dc.typeMakale
dc.relation.journalPEDIATRIC NEPHROLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume29
dc.identifier.issue9
dc.identifier.startpage1834
dc.identifier.endpage1834
dc.contributor.firstauthorID80778


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