A novel CYP11B1 mutation in a Turkish patient with 11 beta-hydroxylase deficiency: An association with the severe hypokalemia leading to rhabdomyolysis

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dc.contributor.authorYurekli, Banu Sarer
dc.contributor.authorKutbay, Nilufer Ozdemir
dc.contributor.authorOnay, Huseyin
dc.contributor.authorSimsir, Ilgin Yildirim
dc.contributor.authorKocabas, Gokcen Unal
dc.contributor.authorErdogan, Mehmet
dc.contributor.authorCetinkalp, Sevki
dc.contributor.authorOzgen, Gokhan
dc.contributor.authorSaygili, Fusun
dc.date.accessioned2019-10-27T23:10:26Z
dc.date.available2019-10-27T23:10:26Z
dc.date.issued2016
dc.departmentEge Üniversitesien_US
dc.identifier.doi10.14310/horm.2002.1654en_US
dc.identifier.endpage302en_US
dc.identifier.issn1109-3099
dc.identifier.issue2en_US
dc.identifier.pmid27376433en_US
dc.identifier.startpage300en_US
dc.identifier.urihttps://doi.org/10.14310/horm.2002.1654
dc.identifier.urihttps://hdl.handle.net/11454/52893
dc.identifier.volume15en_US
dc.identifier.wosWOS:000378833900017en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherHellenic Endocrine Socen_US
dc.relation.ispartofHormones-International Journal of Endocrinology and Metabolismen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subject11-B hydroxylase deficiencyen_US
dc.subjectHypokalemiaen_US
dc.subjectNovel mutationen_US
dc.titleA novel CYP11B1 mutation in a Turkish patient with 11 beta-hydroxylase deficiency: An association with the severe hypokalemia leading to rhabdomyolysisen_US
dc.typeLetteren_US

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