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
Additional information
The online version of the original article can be found at 10.1038/ejhg.2012.172
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Shanks, M., Downes, S., Copley, R. et al. Erratum: Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease. Eur J Hum Genet 21, 1031 (2013). https://doi.org/10.1038/ejhg.2013.91
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DOI: https://doi.org/10.1038/ejhg.2013.91