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dc.contributor.authorÖzçelik, T.en_US
dc.contributor.authorOnat, O. E.en_US
dc.date.accessioned2019-02-07T10:14:07Z
dc.date.available2019-02-07T10:14:07Z
dc.date.issued2016-09en_US
dc.identifier.issn1061-4036
dc.identifier.urihttp://hdl.handle.net/11693/49011
dc.description.abstractStudy of the Greater Middle East (GME), home to approximately 10% of the world's population, has made invaluable contributions to the characterization of rare genetic disease, especially recessive conditions arising from the tradition of consanguinity and large families with multiple children. A new study now reports 1,111 unrelated exomes from the GME and provides a comprehensive view of genetic variation for enhanced discovery of disease-associated genes.en_US
dc.language.isoEnglishen_US
dc.source.titleNature Geneticsen_US
dc.relation.isversionofhttps://doi.org/10.1038/ng.3652en_US
dc.subjectConsanguinityen_US
dc.subjectGenesen_US
dc.subjectRecessiveen_US
dc.subjectGenetic variationen_US
dc.subjectGenomicsen_US
dc.subjectHumansen_US
dc.subjectMiddle Easten_US
dc.titleGenomic landscape of the Greater Middle Easten_US
dc.typeArticleen_US
dc.departmentDepartment of Molecular Biology and Geneticsen_US
dc.departmentInstitute of Materials Science and Nanotechnology (UNAM)en_US
dc.departmentNanotechnology Research Center (NANOTAM)en_US
dc.citation.spage978en_US
dc.citation.epage979en_US
dc.citation.volumeNumber48en_US
dc.citation.issueNumber9en_US
dc.identifier.doi10.1038/ng.3652en_US
dc.publisherNature Publishing Groupen_US
dc.identifier.eissn1546-1718


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