Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations.


Journal

Genetics in medicine : official journal of the American College of Medical Genetics
ISSN: 1530-0366
Titre abrégé: Genet Med
Pays: United States
ID NLM: 9815831

Informations de publication

Date de publication:
Aug 2019
Historique:
pubmed: 10 10 2018
medline: 10 10 2018
entrez: 10 10 2018
Statut: ppublish

Résumé

The original version of this Article contained an error in the spelling of the author Anja K. Mayer, which was incorrectly given as Anja Kathrin Mayer. This has now been corrected in both the PDF and HTML versions of the Article.

Identifiants

pubmed: 30297699
doi: 10.1038/s41436-018-0305-0
pii: S1098-3600(21)01599-9
pmc: PMC7609298
doi:

Types de publication

Published Erratum

Langues

eng

Sous-ensembles de citation

IM

Pagination

1998

Investigateurs

James R Lupski (JR)
Claudia Carvalho (C)
Max van Min (M)
Petra Klous (P)
Sarah De Jaegere (S)
Sally Hooghe (S)

Commentaires et corrections

Type : ErratumFor

Auteurs

Kristof Van Schil (K)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.

Sarah Naessens (S)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.

Stijn Van de Sompele (S)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.

Marjolein Carron (M)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.

Alexander Aslanidis (A)

Laboratory for Experimental Immunology of the Eye, Department of Ophthalmology, University of Cologne, Cologne, Germany.

Caroline Van Cauwenbergh (C)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.

Anja K Mayer (AK)

Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tuebingen, Tuebingen, Germany.

Mattias Van Heetvelde (M)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.

Miriam Bauwens (M)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.

Hannah Verdin (H)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.

Frauke Coppieters (F)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.

Michael E Greenberg (ME)

Department of Neurobiology, Harvard Medical School, Boston, Massachusetts, USA.

Marty G Yang (MG)

Department of Neurobiology, Harvard Medical School, Boston, Massachusetts, USA.

Marcus Karlstetter (M)

Laboratory for Experimental Immunology of the Eye, Department of Ophthalmology, University of Cologne, Cologne, Germany.

Thomas Langmann (T)

Laboratory for Experimental Immunology of the Eye, Department of Ophthalmology, University of Cologne, Cologne, Germany.

Katleen De Preter (K)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.

Susanne Kohl (S)

Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tuebingen, Tuebingen, Germany.

Timothy J Cherry (TJ)

Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington, USA.
Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, USA.

Bart P Leroy (BP)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Department of Ophthalmology, Ghent University and Ghent University Hospital, Ghent, Belgium.
Division of Ophthalmology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

Elfride De Baere (E)

Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium. Elfride.DeBaere@UGent.be.

Classifications MeSH