Crossmark

Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

Crossref DOI link: https://doi.org/10.1038/s41436-018-0392-y

Published Print: 2019-04

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

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
License Information

Text and Data Mining valid from 2019-04-01

Text and Data Mining valid from 2019-04-01

Version of Record valid from 2021-11-24
More Information

This article is maintained by: Elsevier

Article Title: Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0392-y

CrossRef DOI link to the associated document: https://doi.org/10.1038/s41436-018-0345-5

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics