Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/6934
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dc.contributor.authorLower, K.en
dc.contributor.authorGecz, J.en
dc.date.issued2001en
dc.identifier.citationAmerican Journal of Medical Genetics. Part A, 2001; 100(1):43-48en
dc.identifier.issn1552-4825en
dc.identifier.issn0148-7299en
dc.identifier.urihttp://hdl.handle.net/2440/6934-
dc.description.abstractBörjeson-Forssman-Lehmann syndrome (BFLS) is a syndromic X-linked mental retardation that has been mapped by linkage to Xq26-q27. A nonsyndromic mental retardation family, MRX27, has also been localized to a region of the X chromosome overlapping Xq26-q27. The gene for ARHGEF6 (also known as alphaPIX or Cool-2), a newly identified guanine nucleotide exchange factor, was identified as a potential candidate XLMR gene, due to its location within the BFLS and MRX27 critical regions and its function in the regulation of PAK3 (a known MRX gene). The full coding sequence and genomic structure of the gene for ARHGEF6 was established in silico, based on available genomic, EST, and cDNA sequence information. Mutation analysis in BFLS- and MRX27-affected individuals was carried out. No mutations were found in two BFLS families or MRX27. Although ARHGEF6 is unlikely to be the gene responsible for either BFLS or MRX27, it remains a prime candidate for nonspecific or syndromic mental retardation linked to Xq26.en
dc.language.isoenen
dc.publisherWiley-Lissen
dc.subjectX Chromosome; Humans; Syndrome; Genetic Predisposition to Disease; Guanine Nucleotide Exchange Factors; Cell Cycle Proteins; DNA; Chromosome Mapping; Sequence Analysis, DNA; DNA Mutational Analysis; Gene Expression; Alternative Splicing; Mutation; Polymorphism, Single Nucleotide; Genes; Introns; Exons; Expressed Sequence Tags; Databases, Factual; Genetic Linkage; Intellectual Disability; Rho Guanine Nucleotide Exchange Factorsen
dc.titleCharacterization of ARHGEF6, a guanine nucleotide exchange factor for Rho GTPases and a candidate gene for x-linked mental retardation: Mutation screening in Borjeson-Forssman-Lehmann syndrome and MRX27en
dc.typeJournal articleen
dc.identifier.rmid0020010883en
dc.identifier.doi10.1002/ajmg.1189en
dc.identifier.pubid61729-
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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