Genomic landscape of the Greater Middle East
dc.citation.epage | 979 | en_US |
dc.citation.issueNumber | 9 | en_US |
dc.citation.spage | 978 | en_US |
dc.citation.volumeNumber | 48 | en_US |
dc.contributor.author | Özçelik, T. | en_US |
dc.contributor.author | Onat, O. E. | en_US |
dc.date.accessioned | 2019-02-07T10:14:07Z | |
dc.date.available | 2019-02-07T10:14:07Z | |
dc.date.issued | 2016-09 | en_US |
dc.department | Department of Molecular Biology and Genetics | en_US |
dc.department | Institute of Materials Science and Nanotechnology (UNAM) | en_US |
dc.department | Nanotechnology Research Center (NANOTAM) | en_US |
dc.description.abstract | Study 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.identifier.doi | 10.1038/ng.3652 | en_US |
dc.identifier.eissn | 1546-1718 | |
dc.identifier.issn | 1061-4036 | |
dc.identifier.uri | http://hdl.handle.net/11693/49011 | |
dc.language.iso | English | en_US |
dc.publisher | Nature Publishing Group | en_US |
dc.relation.isversionof | https://doi.org/10.1038/ng.3652 | en_US |
dc.source.title | Nature Genetics | en_US |
dc.subject | Consanguinity | en_US |
dc.subject | Genes | en_US |
dc.subject | Recessive | en_US |
dc.subject | Genetic variation | en_US |
dc.subject | Genomics | en_US |
dc.subject | Humans | en_US |
dc.subject | Middle East | en_US |
dc.title | Genomic landscape of the Greater Middle East | en_US |
dc.type | Article | en_US |
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