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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.authorsTurkgenc, B.; Temel, S. G.; Uysal, F.; Atik, S. Ugan; Oztunc, F.; Sulu, A.; Ekici, F.; Ayabakan, C.; Odemis, E.; Saygili, A.; Koka, A.; Akinci, I. Ozkan; Alanay, Y.; Celiker, A.; Ozer, A.; Yakicier, M. C.
dc.date.accessioned2022-03-12T16:24:28Z
dc.date.accessioned2026-01-11T17:50:35Z
dc.date.available2022-03-12T16:24:28Z
dc.date.issued2019
dc.identifier.doidoiWOS:000489313101093
dc.identifier.eissn1476-5438
dc.identifier.issn1018-4813
dc.identifier.urihttps://hdl.handle.net/11424/226353
dc.identifier.wosWOS:000489313101093
dc.language.isoeng
dc.publisherNATURE PUBLISHING GROUP
dc.relation.ispartofEUROPEAN JOURNAL OF HUMAN GENETICS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleNext Generation Sequencing (NGS) panel revealed new candidate genes and variants in 25 Hypertrophic Cardiomyopathy patients
dc.typeconferenceObject
dspace.entity.typePublication
oaire.citation.endPage150
oaire.citation.startPage150
oaire.citation.titleEUROPEAN JOURNAL OF HUMAN GENETICS
oaire.citation.volume27

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