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A rare cause of hypertension in childhood: Answers

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dc.contributor.authorBEREKET, ABDULLAH
dc.contributor.authorDEMİRCİOĞLU, SERAP
dc.contributor.authorGÜRAN, TÜLAY
dc.contributor.authorsKucuk, Nuran; Abali, Zehra Yavas; Abali, Saygin; Canpolat, Nur; Yesil, Gozde; Turan, Serap; Bereket, Abdullah; Guran, Tulay
dc.date.accessioned2022-03-10T11:19:59Z
dc.date.accessioned2026-01-11T08:51:19Z
dc.date.available2022-03-10T11:19:59Z
dc.date.issued2020
dc.identifier.doi10.1007/s00467-019-04329-0
dc.identifier.eissn1432-198X
dc.identifier.issn0931-041X
dc.identifier.pubmed31541304
dc.identifier.urihttps://hdl.handle.net/11424/219704
dc.identifier.wosWOS:000509700100012
dc.language.isoeng
dc.publisherSPRINGER
dc.relation.ispartofPEDIATRIC NEPHROLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectLow renin hypertension
dc.subjectApparent mineralocorticoid excess
dc.subjectHSD11B2 gene
dc.subjectAPPARENT MINERALOCORTICOID EXCESS
dc.subjectMUTATION
dc.subjectGENE
dc.titleA rare cause of hypertension in childhood: Answers
dc.typeeditorial
dspace.entity.typePublication
oaire.citation.endPage82
oaire.citation.issue1
oaire.citation.startPage79
oaire.citation.titlePEDIATRIC NEPHROLOGY
oaire.citation.volume35

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