Analysis of Hpse2 Gene Mutations in Children with Non-neurogenic Neurogenic Bladder and Urofacial (ochoa) Syndrome

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dc.contributor.authorBulum, Burcu
dc.contributor.authorOzCakar, Z. Birsin
dc.contributor.authorDuman, Duygu
dc.contributor.authorCengiz, Filiz Basak
dc.contributor.authorBurgu, Berk
dc.contributor.authorCakar, Nilgun
dc.contributor.authorBaskin, Esra
dc.contributor.authorSoygur, Tarkan
dc.contributor.authorEkim, Mesiha
dc.contributor.authorTekin, Mustafa
dc.contributor.authorYalcinkaya, Fatos
dc.contributor.orcIDhttps://orcid.org/0000-0003-4361-8508en_US
dc.contributor.researcherIDB-5785-2018en_US
dc.date.accessioned2023-12-29T13:14:48Z
dc.date.available2023-12-29T13:14:48Z
dc.date.issued2014
dc.identifier.endpage1698en_US
dc.identifier.issn0931-041Xen_US
dc.identifier.issue9en_US
dc.identifier.startpage1698en_US
dc.identifier.urihttp://hdl.handle.net/11727/11264
dc.identifier.volume29en_US
dc.identifier.wos000341377700145en_US
dc.language.isoengen_US
dc.relation.journalPEDIATRIC NEPHROLOGYen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleAnalysis of Hpse2 Gene Mutations in Children with Non-neurogenic Neurogenic Bladder and Urofacial (ochoa) Syndromeen_US
dc.typeconferenceObjecten_US

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