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dc.contributor.authorKleanthous, Mariosen
dc.contributor.authorPatsalis, Philippos C.en
dc.contributor.authorDrousiotou, Anthien
dc.contributor.authorMotazacker, M.en
dc.contributor.authorChristodoulou, Kyproulaen
dc.contributor.authorCariolou, Marios A.en
dc.contributor.authorBaysal, E.en
dc.contributor.authorKhrizi, K.en
dc.contributor.authorMoghimi, B.en
dc.contributor.authorPourfarzad, F.en
dc.contributor.authorvan Baal, S.en
dc.contributor.authorConstantinou-Deltas, Constantinos D.en
dc.contributor.authorNajmabadi, H.en
dc.contributor.authorPatrinos, G. P.en
dc.creatorKleanthous, Mariosen
dc.creatorPatsalis, Philippos C.en
dc.creatorDrousiotou, Anthien
dc.creatorMotazacker, M.en
dc.creatorChristodoulou, Kyproulaen
dc.creatorCariolou, Marios A.en
dc.creatorBaysal, E.en
dc.creatorKhrizi, K.en
dc.creatorMoghimi, B.en
dc.creatorPourfarzad, F.en
dc.creatorvan Baal, S.en
dc.creatorConstantinou-Deltas, Constantinos D.en
dc.creatorNajmabadi, H.en
dc.creatorPatrinos, G. P.en
dc.date.accessioned2019-11-04T12:52:11Z
dc.date.available2019-11-04T12:52:11Z
dc.date.issued2006
dc.identifier.issn1098-1004
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/53185
dc.description.abstractThe National Mutation Frequency Databases are continuously updated mutation depositories, which contain extensive information over the described genetic heterogeneity of an ethnic group or population. Here, we report the construction of the Cypriot (http://www.goldenhelix.org/cypriot) and Iranian National Mutation Frequency Databases (http://www.goldenhelix.org/iranian), both derived from an academic effort to provide high quality and up-to-date information on the underlying genetic heterogeneity of inherited disorders in the Cypriot and Iranian populations, respectively. Both databases have been built and maintained online using ETHNOS platform, a specialized software, which provides the means for national mutation database construction and curation. Each database contains brief summaries of the various genetic disorders studied for each population, and an easy-to-use query interface provides, both to specialist as well as to non-specialist users (i.e. patients and their families), instant access to the list and frequencies of the different mutations responsible for the inherited disorders in these populations. Furthermore, numerous links to the respective Online Mendelian Inheritance in Man (OMIM) entries and, when available, to the locus-specific databases fruitfully integrate the databases content into a single Web site. Both databases can serve as valuable online tools for molecular genetic testing of inherited disorders in these populations and could potentially motivate further investigations of yet unknown genetic diseases in the Cypriot and Iranian populations.en
dc.sourceHuman mutation.en
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-33745322405&partnerID=40&md5=801649eb06a4973592e28158070f03fb
dc.subjectCyprusen
dc.subjectarticleen
dc.subjectgene frequencyen
dc.subjectgeneticsen
dc.subjectmutationen
dc.subjectgenetic screeningen
dc.subjectgenetic disorderen
dc.subjectpopulation geneticsen
dc.subjectGenetics, Populationen
dc.subjectDatabases, Geneticen
dc.subjectgenetic databaseen
dc.subjectGenetic Diseases, Inbornen
dc.subjectIranen
dc.titleThe cypriot and Iranian National Mutation Frequency Databases.en
dc.typeinfo:eu-repo/semantics/article
dc.description.volume27
dc.description.startingpage598
dc.description.endingpage599
dc.author.facultyΣχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Βιολογικών Επιστημών / Department of Biological Sciences
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :15</p>en
dc.source.abbreviationHum.Mutat.en
dc.contributor.orcidConstantinou-Deltas, Constantinos D. [0000-0001-5549-9169]
dc.gnosis.orcid0000-0001-5549-9169


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