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THE FIRST CASE OF AMYLOIDOSIS DUE TO HOMOZYGOUS P.V377I MUTATION IN A PATIENT WITH HYPERIMMUNOGLOBULIN D SYNDROME

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dc.contributor.authorsBodur, Ece Demirci; Gokce, Ibrahim; Sozeri, Betul; Alavanda, Ceren; Farmanli, Orkhan; Ata, Pinar; Kaya, Handan; Alpay, Harika
dc.date.accessioned2022-03-10T18:02:09Z
dc.date.accessioned2026-01-10T18:44:18Z
dc.date.available2022-03-10T18:02:09Z
dc.date.issued2021
dc.identifier.doidoiWOS:000696562600499
dc.identifier.eissn1432-198X
dc.identifier.issn0931-041X
dc.identifier.urihttps://hdl.handle.net/11424/222397
dc.identifier.wosWOS:000696562600499
dc.language.isoeng
dc.publisherSPRINGER
dc.relation.ispartofPEDIATRIC NEPHROLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleTHE FIRST CASE OF AMYLOIDOSIS DUE TO HOMOZYGOUS P.V377I MUTATION IN A PATIENT WITH HYPERIMMUNOGLOBULIN D SYNDROME
dc.typeconferenceObject
dc.type.submeetingabstract
dspace.entity.typePublication
oaire.citation.endPage3448
oaire.citation.issue10
oaire.citation.startPage3448
oaire.citation.titlePEDIATRIC NEPHROLOGY
oaire.citation.volume36

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