Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/2558
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dc.contributor.authorStevanović, Milenaen_US
dc.contributor.authorLovell-badge, Robinen_US
dc.contributor.authorCollignon, Jérmeen_US
dc.contributor.authorGoodfellow, Peter N.en_US
dc.date.accessioned2019-10-24T19:33:13Z-
dc.date.available2019-10-24T19:33:13Z-
dc.date.issued1993-12-
dc.identifier.issn0964-6906-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/2558-
dc.description.abstractThe mammallan genome contains a family of genes that are related to SRY, the mammalian sex determining gene. The homology is restricted to the region of SRY that encodes a DNA binding motif of the HMG-box class. These genes have been named SOX genes (SRY-related HMG-box genes). We have cloned and characterised SOX3, a member of the human SOX gene family. SOX3 maps to the X chromosome in the region Xq26-27. A mentally retarded male patient with haemophilia B Is deleted for both the Factor lX gene and SOX3. This suggests that SOX3 Is not essential for testis formation. The phenotype of the patient and the expression of SOX3 gene in neuronal tissues raises the possibility that this gene is a candidate gene for Borjeson-Forssman-Lehmann, an X-llnked mental retardation syndrome. © 1993 Oxford University Press.en_US
dc.language.isoenen_US
dc.relation.ispartofHuman Molecular Geneticsen_US
dc.titleSOX3 is an X-linked gene related to SRYen_US
dc.typeArticleen_US
dc.identifier.doi10.1093/hmg/2.12.2013-
dc.identifier.pmid8111369-
dc.identifier.scopus2-s2.0-0027752708-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/0027752708-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0003-4286-7334-
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