Correction to: Journal of Human Genetics
The original version of this article unfortunately contained a mistake. In the article, we described a “new” ATP7B variant (p.R816S) as a common mutation in Upper Austria, mistakenly considering the last 3 nucleotides of exon 9 to code for Arginine. In fact, the third nucleotide is the first of the adjacent intron. Reanalysis of the sample by NGS showed that this variant was in fact 2447+1G>T. This variant is listed as likely pathogenic in ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/).
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Hofer, H., Willheim-Polli, C., Knoflach, P. et al. Correction: Identification of a novel Wilson disease gene mutation frequent in Upper Austria: a genetic and clinical study. J Hum Genet 66, 1199 (2021). https://doi.org/10.1038/s10038-021-00918-w
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DOI: https://doi.org/10.1038/s10038-021-00918-w
