Novel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferens

Basit Öğe Kaydı
dc.authorid0000-0001-7914-2201en_US
dc.contributor.authorAkın, Y.
dc.contributor.authorDemir, Deniz
dc.contributor.authorGörgişen, G.
dc.contributor.authorLüleci, G.
dc.contributor.authorAlper, O.M.
dc.contributor.authorWatanabe, C.S.
dc.contributor.authorSahiner, I.F.
dc.contributor.authorUsta, M.F.
dc.contributor.authorDemir, Deniz
dc.date.accessioned2024-07-12T21:01:10Z
dc.date.available2024-07-12T21:01:10Z
dc.date.issued2014en_US
dc.departmentFakülteler, Tıp Fakültesien_US
dc.description.abstractNovel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferensen_US
dc.identifier.citationAkın, Y., Demir, D., Görgişen, G., Lüleci, G., Alper, O.M., Watanabe, C.S., Sahiner, I.F. ve Usta, M.F. (2014). Novel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferens. Andrologia, Wiley Online Library. 46(2), s. 198-199.en_US
dc.identifier.endpage199en_US
dc.identifier.issn1439-0272
dc.identifier.issue2en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage198en_US
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/23240968/
dc.identifier.urihttps://hdl.handle.net/20.500.12415/3461
dc.identifier.volume46en_US
dc.institutionauthorDemir, Deniz
dc.language.isoenen_US
dc.publisherWiley Online Libraryen_US
dc.relation.ispartofAndrologiaen_US
dc.relation.isversionof10.1111/and.12053en_US
dc.relation.publicationcategoryUluslararası Hakemli Dergide Makale - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.snmzKY07238
dc.titleNovel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferensen_US
dc.typeConference Object
dspace.entity.typePublication

Dosyalar

Koleksiyon

Tıp Fakültesi Koleksiyonu