Yayın:
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.authorKorkmaz, C.
dc.contributor.authorKilinc, A. Ayzit
dc.contributor.authorSavas, S.
dc.contributor.authorErcan, F.
dc.contributor.authorKosak, S.
dc.contributor.authorKarcioglu, O.
dc.contributor.authorGulen, F.
dc.contributor.authorOzturk, G. Kartal
dc.contributor.authorCanitez, Y.
dc.contributor.authorKorkmaz, M.
dc.contributor.authorTalip, M.
dc.contributor.authorKose, M.
dc.contributor.authorErsoy, A.
dc.contributor.authorTural, D. Ademhan
dc.contributor.authorYetisgin, H.
dc.contributor.authorKeskin, O.
dc.contributor.authorInal, G.
dc.contributor.authorHangul, M.
dc.contributor.authorDagdelen, E. Cagri
dc.contributor.authorBingol, A.
dc.contributor.authorBasaran, A. E.
dc.contributor.authorOzdemir, A.
dc.contributor.authorYulug, D. Polat
dc.contributor.authorSerbes, M.
dc.contributor.authorAltintas, D. U.
dc.contributor.authorKekec, H.
dc.contributor.authorAslan, A. T.
dc.contributor.authorOzsezen, B.
dc.contributor.authorGursoy, T. Ramasli
dc.contributor.authorCobanoglu, N.
dc.contributor.authorKorkmaz, P.
dc.contributor.authorYuksel, H.
dc.contributor.authorAnil, H.
dc.contributor.authorAydin, Z. G. Gayretli
dc.contributor.authorAsfuroglu, P.
dc.contributor.authorCaltepe, G.
dc.contributor.authorDemirdogen, E.
dc.contributor.authorKilic, M.
dc.contributor.authorTopal, E.
dc.contributor.authorHizal, M.
dc.contributor.authorCakar, E. P.
dc.contributor.authorIkizoglu, N. Bas
dc.contributor.authorBuyuksahin, H. Nayir
dc.contributor.authorZirek, F.
dc.contributor.authorOcak, E.
dc.contributor.authorCakir, E.
dc.contributor.authorEyupoglu, T. Sismanlar
dc.contributor.authorCinel, G.
dc.contributor.authorPekcan, S.
dc.contributor.authorOrdukaya, N. Emiralioglu
dc.contributor.authorDogru, D.
dc.contributor.authorOzcelik, U.
dc.contributor.authorErden, D. Dayangac
dc.contributor.buuauthorDEMİRDÖĞEN, EZGİ
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentGöğüs Hastalıkları Ana Bilim Dalı
dc.contributor.researcheridMZF-8838-2025
dc.date.accessioned2025-11-06T17:07:03Z
dc.date.issued2025-07-01
dc.identifier.endpage430
dc.identifier.issn2211-5463
dc.identifier.startpage430
dc.identifier.urihttps://hdl.handle.net/11452/56784
dc.identifier.volume15
dc.identifier.wos001552034504203
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherWiley
dc.relation.journalFebs open bio
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectBiochemistry & Molecular Biology
dc.titleIn silico analyses of rare CFTR variants from the Turkish national cystic fibrosis patient registry to predict their functional effects
dc.typeMeeting Abstract
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Göğüs Hastalıkları Ana Bilim Dalı
local.indexed.atWOS
relation.isAuthorOfPublication2445e2a7-e9d2-4c20-b3a7-84945617a6a0
relation.isAuthorOfPublication.latestForDiscovery2445e2a7-e9d2-4c20-b3a7-84945617a6a0

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