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Targeted custom gene panel sequencing for cardiac ion channelopathies: Efficiently detects candidate pathogenic mutations in Long QT syndrome

dc.contributor.buuauthorTemel, Şehime Gülsün
dc.contributor.buuauthorUysal, Fahrettin
dc.contributor.buuauthorBostan, O. M.
dc.contributor.buuauthorÇil, Ergün
dc.contributor.departmentTıp Fakültesi
dc.contributor.researcheridAAG-8385-2021
dc.contributor.researcheridAAH-4421-2021
dc.date.accessioned2023-07-31T07:39:32Z
dc.date.available2023-07-31T07:39:32Z
dc.date.issued2017-08-30
dc.descriptionBu çalışma, 25-27, Mayıs 2017 tarihlerinde Dubrovnik[Hırvatistan]’da düzenlenen European Biotechnology Congress Kongresi‘nde bildiri olarak sunulmuştur.
dc.descriptionÇalışmada 27 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının girişleri yapılmıştır.
dc.description.sponsorshipSANTEZ Project, Turkey - 0253.STZ.2013-2
dc.identifier.citationTemel, Ş. G. vd. (2017). ''Targeted custom gene panel sequencing for cardiac ion channelopathies: Efficiently detects candidate pathogenic mutations in Long QT syndrome''. Journal of Biotechnology, 256(Supplement S), S28-S29.
dc.identifier.doi10.1016/j.jbiotec.2017.06.647
dc.identifier.endpageS26
dc.identifier.issn0168-1656
dc.identifier.issn1873-4863
dc.identifier.issueSupplement S
dc.identifier.startpageS28
dc.identifier.urihttps://doi.org/10.1016/j.jbiotec.2017.06.647
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0168165617309434
dc.identifier.urihttp://hdl.handle.net/11452/33331
dc.identifier.volume256
dc.identifier.wos000413585400083
dc.indexed.wosSCIE
dc.indexed.wosSSCI
dc.language.isoen
dc.publisherElsevier
dc.relation.collaborationYurt içi
dc.relation.collaborationSanayi
dc.relation.journalJournal of Biotechnology
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBiotechnology & applied microbiology
dc.subject.wosBiotechnology & applied microbiology
dc.titleTargeted custom gene panel sequencing for cardiac ion channelopathies: Efficiently detects candidate pathogenic mutations in Long QT syndrome
dc.typeOther
dc.type.subtypeMeeting Abstract
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi
local.indexed.atWOS

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