Next Generation Sequencing (NGS) panel revealed new candidate genes and variants in 25 Hypertrophic Cardiomyopathy patients

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dc.contributor.authorTurkgenc, B.
dc.contributor.authorTemel, S. G.
dc.contributor.authorUysal, F.
dc.contributor.authorAtik, S. Ugan
dc.contributor.authorOztunc, F.
dc.contributor.authorSulu, A.
dc.contributor.authorEkici, F.
dc.contributor.authorAyabakan, C.
dc.contributor.authorOdemis, E.
dc.contributor.authorSaygili, A.
dc.contributor.authorKoka, A.
dc.contributor.authorAkinci, I. Ozkan
dc.contributor.authorAlanay, Y.
dc.contributor.authorCeliker, A.
dc.contributor.authorOzer, A.
dc.contributor.authorYakicier, M. C.
dc.date.accessioned2025-10-16T15:23:20Z
dc.date.issued2019
dc.description.abstract51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, ITALY, JUN 16-19, 2018
dc.identifier.otherWOS:000489313101093
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/7971
dc.publisherNATURE PUBLISHING GROUP
dc.sourceEUROPEAN JOURNAL OF HUMAN GENETICS
dc.titleNext Generation Sequencing (NGS) panel revealed new candidate genes and variants in 25 Hypertrophic Cardiomyopathy patients
dc.typeMeeting Abstract

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