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Next generation sequencing (NGS) panel revealed new candidate genes and variants in 25 hypertrophic cardiomyopathy patients

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dc.contributor.authorTürkgenç, B.
dc.contributor.authorTemel, Şehime Gülsün
dc.contributor.authorUysal, Fahrettin
dc.contributor.authorAtik, S. Ugan
dc.contributor.authorÖztunç, F.
dc.contributor.authorSulu, A.
dc.contributor.authorEkici, F.
dc.contributor.authorAyabakan, C.
dc.contributor.authorÖdemiş, E.
dc.contributor.authorSaygili, A.
dc.contributor.authorKoka, A.
dc.contributor.authorAkıncı, I. Ozkan
dc.contributor.authorAlanay, Y.
dc.contributor.authorÇeliker, A.
dc.contributor.authorÖzer, A.
dc.contributor.authorYakıcier, M. C.
dc.contributor.buuauthorTEMEL, ŞEHİME GÜLSÜN
dc.contributor.buuauthorUYSAL, FAHRETTİN
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentPediatri Bölümü
dc.contributor.researcheridAAH-4421-2021
dc.contributor.researcheridAAG-8385-2021
dc.date.accessioned2024-11-27T06:05:56Z
dc.date.available2024-11-27T06:05:56Z
dc.date.issued2019-07-01
dc.descriptionBu çalışma, 16-19, Haziran 2018 tarihlerinde Location Milan[İtalya]’da düzenlenen 51. Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) Kongresi‘nde bildiri olarak sunulmuştur.
dc.description.sponsorshipEuropean Soc Human Genet
dc.identifier.eissn1476-5438
dc.identifier.endpage150
dc.identifier.issn1018-4813
dc.identifier.startpage150
dc.identifier.urihttps://hdl.handle.net/11452/48548
dc.identifier.volume27
dc.identifier.wos000489313101093
dc.indexed.wosWOS.SCI
dc.indexed.wosWOS.ISTP
dc.language.isoen
dc.publisherNature Publishing Group
dc.relation.journalEuropean Journal of Human Genetics
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectBiochemistry & molecular biology
dc.subjectGenetics & heredity
dc.titleNext generation sequencing (NGS) panel revealed new candidate genes and variants in 25 hypertrophic cardiomyopathy patients
dc.typeOther
dc.type.subtypeMeeting Abstract
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Pediatri Bölümü
local.contributor.departmentTıp Fakültesi/Embriyoloji Bölümü
local.indexed.atWOS
relation.isAuthorOfPublicationf513efaa-a54e-4cfa-840f-28e2fbdc001a
relation.isAuthorOfPublication3f01723b-f726-41a2-8b35-aafd1a9b1703
relation.isAuthorOfPublication.latestForDiscoveryf513efaa-a54e-4cfa-840f-28e2fbdc001a

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