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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
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Bélgica
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Bélgica