Published in Volume
121, Issue 2
(February 1, 2011)J Clin Invest.
Copyright © 2011, American Society for Clinical
PDZD7 is a modifier of retinal disease and a
contributor to digenic Usher syndrome
Published February 1, 2011
Original citation: J. Clin. Invest. 2010;120(6):1812–1823.
Citation for this clarification: J. Clin. Invest. 2011;121(2):821.
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.