Inactivating Mutations in CCDC141 Causing Idiopathic Hypogonadotrophic Hypogonadism/Kallmann Syndrome

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dc.contributor.authorTuran, Ihsan
dc.contributor.authorHutchins, B. Ian
dc.contributor.authorHacihamdioglu, Bulent
dc.contributor.authorOzbek, Mehmet Nuri
dc.contributor.authorKotan, Leman Damla
dc.contributor.authorOzkan, Yusuf
dc.contributor.authorTopaloglu, Kemal
dc.date.accessioned2026-08-12T18:13:26Z
dc.date.issued2016
dc.departmentFırat Üniversitesi
dc.description.abstract[Abstract Not Available]
dc.identifier.endpage58
dc.identifier.issn1663-2818
dc.identifier.issn1663-2826
dc.identifier.startpage58
dc.identifier.urihttps://hdl.handle.net/11508/64398
dc.identifier.volume86
dc.identifier.wosWOS:000384166800138
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherKarger
dc.relation.ispartofHormone Research in Paediatrics
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.titleInactivating Mutations in CCDC141 Causing Idiopathic Hypogonadotrophic Hypogonadism/Kallmann Syndrome
dc.typeConference Object

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