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Clarification

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

Inga Ebermann, Jennifer B. Phillips, Max C. Liebau, Robert K. Koenekoop, Bernhard Schermer, Irma Lopez, Ellen Schäfer, Anne-Francoise Roux, Claudia Dafinger, Antje Bernd, Eberhart Zrenner, Mireille Claustres, Bernardo Blanco, Gudrun Nürnberg, Peter Nürnberg, Rebecca Ruland, Monte Westerfield, Thomas Benzing and Hanno J. Bolz

Published February 1, 2011

Original citation: J. Clin. Invest. 2010;120(6):1812–1823. doi:10.1172/JCI39715.

Citation for this clarification: J. Clin. Invest. 2011;121(2):821. doi:10.1172/JCI46312.

Since the article was published, the zebrafish genome assembly has been updated from zv8 to zv9, and the exon numbers have changed. The ush2a GT sequence (5′-GTACGACCTTATGCTTACCTGTTGG-3′) was originally thought to target the splice donor site of exon 6, but it has been updated to exon 4 of ush2a, as annotated in the Ensembl transcript ID ENSDART00000086201.

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