Correction to: Journal of Human Genetics https://doi.org/10.1038/s10038-024-01219-8, published online 17 January 2024
The patient variant described on pages 144–146 is accurately stated as follows: compound heterozygous ABCA2 variants, NM_001606.5:c.[5300–17C>A];[6379C>T] p.[Tyr1766_Gly1767insAlaProProCysAla,Ile1768Hisfs*188];[(Gln2127*)]
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Inoue, Y., Tsuchida, N., Kim, C.A. et al. Correction: Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability. J Hum Genet 71, 59–62 (2026). https://doi.org/10.1038/s10038-025-01422-1
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DOI: https://doi.org/10.1038/s10038-025-01422-1
