Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/7340
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dc.contributor.authorBienvenu, T.en
dc.contributor.authorPoirier, K.en
dc.contributor.authorFriocourt, G.en
dc.contributor.authorBahi, N.en
dc.contributor.authorBeaumont, D.en
dc.contributor.authorFauchereau, F.en
dc.contributor.authorJeema, L.en
dc.contributor.authorZemni, R.en
dc.contributor.authorVinet, M.en
dc.contributor.authorFrancis, F.en
dc.contributor.authorCouvert, P.en
dc.contributor.authorGomot, M.en
dc.contributor.authorMoraine, C.en
dc.contributor.authorvan Bokhoven, H.en
dc.contributor.authorKalscheuer, V.en
dc.contributor.authorFrints, S.en
dc.contributor.authorGecz, J.en
dc.contributor.authorOhzaki, K.en
dc.contributor.authorChaabouni, H.en
dc.contributor.authorFryns, J.en
dc.contributor.authoret al.en
dc.date.issued2002en
dc.identifier.citationHuman Molecular Genetics, 2002; 11(8):981-991en
dc.identifier.issn0964-6906en
dc.identifier.issn1460-2083en
dc.identifier.urihttp://hdl.handle.net/2440/7340-
dc.description.abstractInvestigation of a critical region for an X-linked mental retardation (XLMR) locus led us to identify a novel Aristaless related homeobox gene (ARX ). Inherited and de novo ARX mutations, including missense mutations and in frame duplications/insertions leading to expansions of polyalanine tracts in ARX, were found in nine familial and one sporadic case of MR. In contrast to other genes involved in XLMR, ARX expression is specific to the telencephalon and ventral thalamus. Notably there is an absence of expression in the cerebellum throughout development and also in adult. The absence of detectable brain malformations in patients suggests that ARX may have an essential role, in mature neurons, required for the development of cognitive abilities.en
dc.description.statementofresponsibilityThierry Bienvenu, Karine Poirier, Gaelle Friocourt, Nadia Bahi, Delphine Beaumont, Fabien Fauchereau, Lamia Ben Jeema, Ramzi Zemni, Marie-Claude Vinet, Fiona Francis, Philippe Couvert, Marie Gomot, Claude Moraine, Hans van Bokhoven, Vera Kalscheuer, Suzanne Frints, Josef Gecz, Kanae Ohzaki, Habiba Chaabouni, Jean-Pierre Fryns, Vincent Desportes, Cherif Beldjord and Jamel Chellyen
dc.language.isoenen
dc.publisherOxford Univ Pressen
dc.rightsCopyright © 2002 Oxford University Pressen
dc.subjectTelencephalon; Chromosomes, Human, X; Humans; Sex Chromosome Disorders; Peptides; Homeodomain Proteins; Transcription Factors; Pedigree; Sequence Analysis, DNA; Sequence Analysis, Protein; Gene Expression; Amino Acid Sequence; Mutation; Mutation, Missense; Genes, Homeobox; Molecular Sequence Data; Adolescent; Adult; Middle Aged; Child; Child, Preschool; Intellectual Disabilityen
dc.titleARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardationen
dc.typeJournal articleen
dc.identifier.rmid0020021107en
dc.identifier.doi10.1093/hmg/11.8.981en
dc.identifier.pubid59967-
pubs.library.collectionPaediatrics publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]en
Appears in Collections:Paediatrics publications

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