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dc.contributor.authorSteinlein, O.K.
dc.contributor.authorDervent, A.
dc.contributor.authorAǧan, K.
dc.contributor.authorÇokar, Ö.
dc.contributor.authorSaltik, S.
dc.contributor.authorÇaǧlayan, S.H.
dc.contributor.authorYalçin, Ö.
dc.date.accessioned2020-03-18T17:35:01Z
dc.date.available2020-03-18T17:35:01Z
dc.date.issued2007
dc.identifier.urihttps://www.scopus.com/inward/record.url?eid=2-s2.0-38349030840&partnerID=40&md5=e5e44b9c00a71b361db84ceeff620fa5
dc.identifier.urihttp://hdl.handle.net/11424/115872
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleA novel missense mutation (N258S) in the KCNQ2 gene in a Turkish family afflicted with benign familial neonatal convulsions (BFNC)
dc.typeArticle
dc.relation.journalTurkish Journal of Pediatrics
dc.contributor.departmentMarmara Üniversitesi
dc.identifier.volume49
dc.identifier.issue4
dc.identifier.startpage385
dc.identifier.endpage389
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı


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