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A rare cause of nephrotic syndrome: the p.Leu364Pro mutation associated with familial Lesitin Cholesterol Acyl Transferase deficiency

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dc.contributor.coauthorPalit, Fatih
dc.contributor.coauthorTas, Murat Yasar
dc.contributor.coauthorSolakoglu, Seyhun
dc.contributor.coauthorKilicaslan, Isin
dc.contributor.coauthorYildiz, Guersel
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorHasbal, Nuri Barış
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-03-06T21:01:09Z
dc.date.issued2024
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeNational
dc.description.sponsoredbyTubitakEuN/A
dc.identifier.doi10.5152/turkjnephrol.2024.24782
dc.identifier.eissn2667-4440
dc.identifier.issue3
dc.identifier.quartileQ4
dc.identifier.scopus2-s2.0-85198701451
dc.identifier.urihttps://doi.org/10.5152/turkjnephrol.2024.24782
dc.identifier.urihttps://hdl.handle.net/20.500.14288/27964
dc.identifier.volume33
dc.identifier.wos1321389700011
dc.language.isoeng
dc.publisherAVES
dc.relation.ispartofTurkish Journal of Nephrology
dc.subjectUrology and nephrology
dc.titleA rare cause of nephrotic syndrome: the p.Leu364Pro mutation associated with familial Lesitin Cholesterol Acyl Transferase deficiency
dc.typeLetter
dspace.entity.typePublication
local.contributor.kuauthorHasbal, Nuri Barış
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
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