FRA2A is a CGG repeat expansion associated with silencing of AFF3.

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Title: FRA2A is a CGG repeat expansion associated with silencing of AFF3.
Authors: Metsu S; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium., Rooms L; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium., Rainger J; Medical and Developmental Genetics Section, MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, United Kingdom., Taylor MS; Medical and Developmental Genetics Section, MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, United Kingdom., Bengani H; Medical and Developmental Genetics Section, MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, United Kingdom., Wilson DI; University of Southampton, Centre for Human Development, Stem Cells and Regeneration, Human Genetics, Southampton, United Kingdom., Chilamakuri CS; Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway., Morrison H; Medical and Developmental Genetics Section, MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, United Kingdom., Vandeweyer G; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium., Reyniers E; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium., Douglas E; Genetics and Molecular Pathology, SA Pathology, Adelaide, South Australia, Australia., Thompson G; Department of Paediatrics, The University of Adelaide, Adelaide, South Australia, Australia; Department of Paediatrics and Child Health, Flinders University, Adelaide, South Australia, Australia., Haan E; Genetics and Molecular Pathology, SA Pathology, Adelaide, South Australia, Australia; South Australian Clinical Genetic Service, SA Pathology (at Women's and Children's Hospital), Adelaide, South Australia, Australia., Gecz J; Genetics and Molecular Pathology, SA Pathology, Adelaide, South Australia, Australia; Department of Paediatrics, The University of Adelaide, Adelaide, South Australia, Australia., Fitzpatrick DR; Medical and Developmental Genetics Section, MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, United Kingdom., Kooy RF; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Source: PLoS genetics [PLoS Genet] 2014 Apr 24; Vol. 10 (4), pp. e1004242. Date of Electronic Publication: 2014 Apr 24 (Print Publication: 2014).
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: FRA2A is a CGG repeat expansion associated with silencing of AFF3.
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  Data: <searchLink fieldCode="AU" term="%22Metsu+S%22">Metsu S</searchLink>; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Rooms+L%22">Rooms L</searchLink>; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Rainger+J%22">Rainger J</searchLink>; Medical and Developmental Genetics Section, MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Taylor+MS%22">Taylor MS</searchLink>; Medical and Developmental Genetics Section, MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Bengani+H%22">Bengani H</searchLink>; Medical and Developmental Genetics Section, MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Wilson+DI%22">Wilson DI</searchLink>; University of Southampton, Centre for Human Development, Stem Cells and Regeneration, Human Genetics, Southampton, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Chilamakuri+CS%22">Chilamakuri CS</searchLink>; Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.<br /><searchLink fieldCode="AU" term="%22Morrison+H%22">Morrison H</searchLink>; Medical and Developmental Genetics Section, MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Vandeweyer+G%22">Vandeweyer G</searchLink>; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Reyniers+E%22">Reyniers E</searchLink>; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Douglas+E%22">Douglas E</searchLink>; Genetics and Molecular Pathology, SA Pathology, Adelaide, South Australia, Australia.<br /><searchLink fieldCode="AU" term="%22Thompson+G%22">Thompson G</searchLink>; Department of Paediatrics, The University of Adelaide, Adelaide, South Australia, Australia; Department of Paediatrics and Child Health, Flinders University, Adelaide, South Australia, Australia.<br /><searchLink fieldCode="AU" term="%22Haan+E%22">Haan E</searchLink>; Genetics and Molecular Pathology, SA Pathology, Adelaide, South Australia, Australia; South Australian Clinical Genetic Service, SA Pathology (at Women's and Children's Hospital), Adelaide, South Australia, Australia.<br /><searchLink fieldCode="AU" term="%22Gecz+J%22">Gecz J</searchLink>; Genetics and Molecular Pathology, SA Pathology, Adelaide, South Australia, Australia; Department of Paediatrics, The University of Adelaide, Adelaide, South Australia, Australia.<br /><searchLink fieldCode="AU" term="%22Fitzpatrick+DR%22">Fitzpatrick DR</searchLink>; Medical and Developmental Genetics Section, MRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Kooy+RF%22">Kooy RF</searchLink>; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
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        Value: 10.1371/journal.pgen.1004242
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