Correction to: European Journal of Human Genetics (2013) 21, 274-280; doi:10.1038/ejhg.2012.172

The authors would like to apologise for the following errors in Table 2.

Three references cited in Table 2 were absent from the final reference list:

ABCA4 N965S

Sun H, Smallwood PM, Nathans J: Biochemical defects in ABCR protein variants associated with human retinopathies. Nat Genet 2000; 26: 242–246.

CRX Y258X

Chau KY, Chen S, Zack DJ, Ono SJ: Functional domains of the cone-rod homeobox (CRX) transcription factor. J Biol Chem 2000; 275: 37264–37270.

GUCY2D R838H

Wilkie SE, Newbold RJ, Deery E et al: Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy. Hum Mol Genet 2000; 9: 3065–3073.

The dbSNP entry rs61749449 refers to N965D rather than N965S.

CRB1T, 745K should read CRB1, T745K.

Also, the following errors were found in Supplementary Table 2:

ABCA4 c.322C>T should read c.3322C>T

ABCA4 c.5882G>C should read c.5882G>A

ABCA4 c.6379C>T should read c.6391G>A

PRPF8 c.6926T>G should read c.6926A>C