A novel missense mutation in SLC12A3 gene in two siblings with Gitelman syndrome

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dc.authorid0000-0002-6280-4587en_US
dc.authorid0000-0001-6189-582Xen_US
dc.contributor.authorTayfur, Aslı Çelebi
dc.contributor.authorMeral, Zehra
dc.contributor.authorYoldaş, Meyri Arzu
dc.date.accessioned2023-11-14T13:02:12Z
dc.date.available2023-11-14T13:02:12Z
dc.date.issued2022en_US
dc.departmentBAİBÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.description.abstractTayfur, A. C., Meral, Z., & Yoldas, M. A. (2022, November). A NOVEL MISSENSE MUTATION IN SLC12A3 GENE IN TWO SIBLINGS WITH GITELMAN SYNDROME. In PEDIATRIC NEPHROLOGY (Vol. 37, No. 11, pp. 2943-2944).en_US
dc.identifier.citationTayfur, A. C., Meral, Z., & Yoldas, M. A. (2022, November). A NOVEL MISSENSE MUTATION IN SLC12A3 GENE IN TWO SIBLINGS WITH GITELMAN SYNDROME. In PEDIATRIC NEPHROLOGY (Vol. 37, No. 11, pp. 2943-2944).en_US
dc.identifier.endpage2944en_US
dc.identifier.issn0931-041X
dc.identifier.issn1432-198X
dc.identifier.issue11en_US
dc.identifier.startpage2943en_US
dc.identifier.urihttps://www.webofscience.com/wos/woscc/full-record/WOS:000855808600411
dc.identifier.urihttps://hdl.handle.net/20.500.12491/11832
dc.identifier.volume37en_US
dc.identifier.wosWOS:000855808600411en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.institutionauthorTayfur, Aslı Çelebi
dc.institutionauthorMeral, Zehra
dc.institutionauthorYoldaş, Meyri Arzu
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofPediatric Nephrologyen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSLC12A3 Geneen_US
dc.subjectMutationen_US
dc.subjectGitelman Syndromeen_US
dc.titleA novel missense mutation in SLC12A3 gene in two siblings with Gitelman syndromeen_US
dc.typeConference Objecten_US

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