A novel missense KCNJ2 gene mutation associated with andersen tawil syndrome

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dc.contributor.authorSözügüzel, Mavi Deniz
dc.contributor.authorIşık, Fatma Büşra
dc.contributor.authorGenç, Nimetullah Mete
dc.contributor.authorÇaralan, E. F.
dc.contributor.authorDoğru, Zübeyir
dc.contributor.authorAkdeniz, Coşkun
dc.contributor.authorCangül, Hakan
dc.date.accessioned2019-12-30T09:34:56Z
dc.date.available2019-12-30T09:34:56Z
dc.date.issued2019
dc.departmentİstanbul Medipol Üniversitesi, Uluslararası Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyoloji Ana Bilim Dalı
dc.descriptionConference: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) Location: Milan, ITALY Date: JUN 16-19, 2018
dc.description.abstract[Abstract Not Available]
dc.description.sponsorshipEuropean Society of Human Geneticsen_US
dc.identifier.citationSözügüzel, M. D., Işık, F. B., Genç, N., Caralan, E. F., Doğru, Z., Akdeniz, C. ... Cangül, H. (2019). A novel missense KCNJ2 gene mutation associated with andersen tawil syndrome. 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) içinde (918-918. ss.). Milan, Italy, June 16-19, 2018.
dc.identifier.endpage918
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.issueSupplement: 1
dc.identifier.startpage918
dc.identifier.urihttps://hdl.handle.net/20.500.12511/4799
dc.identifier.volume27
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherNature Publishing Group
dc.relation.ispartof51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)en_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAndersen Tawil Syndrome
dc.subjectMissense
dc.subjectKCNJ2
dc.titleA novel missense KCNJ2 gene mutation associated with andersen tawil syndrome
dc.typeConference Object

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