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Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.
Van de Sompele, Stijn; Smith, Claire; Karali, Marianthi; Corton, Marta; Van Schil, Kristof; Peelman, Frank; Cherry, Timothy; Rosseel, Toon; Verdin, Hannah; Derolez, Julien; Van Laethem, Thalia; Khan, Kamron N; McKibbin, Martin; Toomes, Carmel; Ali, Manir; Torella, Annalaura; Testa, Francesco; Jimenez, Belen; Simonelli, Francesca; De Zaeytijd, Julie; Van den Ende, Jenneke; Leroy, Bart P; Coppieters, Frauke; Ayuso, Carmen; Inglehearn, Chris F; Banfi, Sandro; De Baere, Elfride.
Afiliação
  • Van de Sompele S; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Smith C; Section of Ophthalmology and Neuroscience, School of Medicine, University of Leeds, St James's University Hospital, Leeds, UK.
  • Karali M; Medical Genetics, Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
  • Corton M; Telethon Institute of Genetics and Medicine, Pozzuoli, Italy.
  • Van Schil K; Genetics Department, Instituto de Investigación Sanitaria-Fundación Jimenez Diaz University Hospital (IIS-FJD, UAM), Madrid, Spain.
  • Peelman F; Center of Biomedical Network Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain.
  • Cherry T; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Rosseel T; Department of Medical Protein Research, Faculty of Medicine and Health Sciences, Flanders Institute for Biotechnology (VIB), Ghent University, Ghent, Belgium.
  • Verdin H; Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA, USA.
  • Derolez J; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Van Laethem T; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Khan KN; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • McKibbin M; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Toomes C; Department of Ophthalmology, St. James's University Hospital, Leeds, UK.
  • Ali M; Department of Ophthalmology, St. James's University Hospital, Leeds, UK.
  • Torella A; Section of Ophthalmology and Neuroscience, School of Medicine, University of Leeds, St James's University Hospital, Leeds, UK.
  • Testa F; Section of Ophthalmology and Neuroscience, School of Medicine, University of Leeds, St James's University Hospital, Leeds, UK.
  • Jimenez B; Medical Genetics, Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
  • Simonelli F; Eye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
  • De Zaeytijd J; Department of Ophthalmology, Fundación Jimenez Diaz University Hospital, Madrid, Spain.
  • Van den Ende J; Eye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
  • Leroy BP; Department of Ophthalmology, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Coppieters F; Center for Medical Genetics, Antwerp University Hospital, Antwerp, Belgium.
  • Ayuso C; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Inglehearn CF; Department of Ophthalmology, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Banfi S; Division of Ophthalmology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • De Baere E; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Genet Med ; 21(4): 1028, 2019 04.
Article em En | MEDLINE | ID: mdl-30607024
The original version of this Article contained an incorrect version of Fig. 3, which included two variants initially shown in black text in Fig. 3a that the authors removed from the final manuscript. The correct version of Fig. 3 without the two variants now appears in the PDF and HTML versions of the Article.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genet Med Ano de publicação: 2019 Tipo de documento: Article
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genet Med Ano de publicação: 2019 Tipo de documento: Article