In silico analyses of rare CFTR variants from The Turkish National Cystic Fibrosis Patient Registry to predict their functional effects

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dc.contributor.authorKara, A. S.
dc.contributor.authorYavuz, B. Capraz
dc.contributor.authorSen, V.
dc.contributor.authorSen, H. Selimoglu
dc.contributor.authorCelebi, O.
dc.contributor.authorOztosun, B.
dc.contributor.authorErden, D. Dayangac
dc.date.accessioned2026-08-12T17:25:56Z
dc.date.issued2025
dc.departmentFırat Üniversitesi
dc.description.abstract[Abstract Not Available]
dc.identifier.endpage430
dc.identifier.issn2211-5463
dc.identifier.startpage430
dc.identifier.urihttps://hdl.handle.net/11508/54616
dc.identifier.volume15
dc.identifier.wosWOS:001552034504203
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofFebs Open Bio
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.titleIn silico analyses of rare CFTR variants from The Turkish National Cystic Fibrosis Patient Registry to predict their functional effects
dc.typeConference Object

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