Publication:
A Case With Novel Missense C.425T>C Mutation in RIPK4 Gene: Bartsocas Papas Syndrome

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dc.authorwosidSeren, Canan/U-7814-2019
dc.contributor.authorYilmaz, A.
dc.contributor.authorKaran, F. I.
dc.contributor.authorAbur, U.
dc.contributor.authorAygun, H. C.
dc.date.accessioned2025-12-11T00:41:04Z
dc.date.issued2020
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Yilmaz, A.] Ondokuz Mayis Univ, Fac Med, Dept Pediat Genet, Samsun, Turkey; [Karan, F. I.; Aygun, H. C.] Ondokuz Mayis Univ, Fac Med, Dept Neonatol, Samsun, Turkey; [Abur, U.] Ondokuz Mayis Univ, Fac Med, Dept Med Genet, Samsun, Turkeyen_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.endpage928en_US
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.scopusqualityQ1
dc.identifier.startpage927en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/38389
dc.identifier.volume28en_US
dc.identifier.wosWOS:000598482603273
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherSpringer Natureen_US
dc.relation.ispartofEuropean Journal of Human Geneticsen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleA Case With Novel Missense C.425T>C Mutation in RIPK4 Gene: Bartsocas Papas Syndromeen_US
dc.typeConference Objecten_US
dspace.entity.typePublication

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