Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/7526
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dc.contributor.authorGecz, J.-
dc.date.issued2000-
dc.identifier.citationJournal of Medical Genetics, 2000; 37(10):782-784-
dc.identifier.issn0022-2593-
dc.identifier.issn1468-6244-
dc.identifier.urihttp://hdl.handle.net/2440/7526-
dc.descriptionCopyright © 2000 by the BMJ Publishing Group Ltd.-
dc.description.abstractWe have identified a novel gene, FMR3, originating from the FRAXE CpG island. The FMR3 gene is transcribed from the opposite strand to the FMR2 gene. Analogous to the silencing of the FMR1 and FMR2 genes, FMR3 transcription is extinguished by FRAXE full mutation. Although the role of FMR3 in FRAXE associated mild to borderline mental retardation is not yet clear, lack of expression of FMR3 in FRAXE full mutation males means that the FMR3 gene is potentially involved.-
dc.language.isoen-
dc.publisherBritish Med Journal Publ Group-
dc.source.urihttp://jmg.bmj.com/cgi/content/abstract/37/10/782-
dc.subjectCentral Nervous System-
dc.subjectX Chromosome-
dc.subjectFibroblasts-
dc.subjectHumans-
dc.subjectFragile X Syndrome-
dc.subjectProteins-
dc.subjectTrans-Activators-
dc.subjectNuclear Proteins-
dc.subjectRNA, Messenger-
dc.subjectRNA, Untranslated-
dc.subjectReverse Transcriptase Polymerase Chain Reaction-
dc.subjectGene Silencing-
dc.subjectGene Deletion-
dc.subjectBase Sequence-
dc.subjectCpG Islands-
dc.subjectTrinucleotide Repeats-
dc.subjectPhenotype-
dc.subjectMutation-
dc.subjectOpen Reading Frames-
dc.subjectIntrons-
dc.subjectExons-
dc.subjectExpressed Sequence Tags-
dc.subjectMolecular Sequence Data-
dc.subjectMale-
dc.subjectGenetic Linkage-
dc.subjectIntellectual Disability-
dc.titleFMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutations-
dc.typeJournal article-
dc.identifier.doi10.1136/jmg.37.10.782-
pubs.publication-statusPublished-
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]-
Appears in Collections:Aurora harvest
Paediatrics publications

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