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Correction to: Compound heterozygous variants including a novel copy number variation in a child with atypical ataxia-telangiectasia: a case report

The Original Article was published on 17 August 2021

Correction to: BMC Med Genomics 14, 204 (2021) https://doi.org/10.1186/s12920-021-01053-3

Following publication of the original article [1], the authors reported an error in Fig. 2.

Figure 2 was replaced as the authors identified an error in part C that was introduced during the peer review process. This error may have affected the interpretation of the results, and therefore, the figure was replaced with the earlier correct version. The original article [1] has been corrected.

Figure 2
figure 2

a Chromatograms of ATM sequence in the proband (top), the patient’s father (middle), and the patient’s mother (bottom) showing an SNV of c.742C > T (p.Arg248Ter) from the father. b Analysis of the next-generation sequencing data using VisCap. c SNP array analysis of the chromosome from the proband (top), the patient’s mother (middle), and the patient’s father (bottom) showing a novel CNV by the deletion of exons 24–40 from the mother. SNV single-nucleotide variation, SNP single-nucleotide polymorphism, CNV copy number variation

Reference

  1. Lee HY, Jang DH, Kim JW, et al. Compound heterozygous variants including a novel copy number variation in a child with atypical ataxia-telangiectasia: a case report. BMC Med Genomics. 2021;14:204. https://doi.org/10.1186/s12920-021-01053-3.

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Correspondence to Dae-Hyun Jang.

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Lee, H.Y., Jang, DH., Kim, JW. et al. Correction to: Compound heterozygous variants including a novel copy number variation in a child with atypical ataxia-telangiectasia: a case report. BMC Med Genomics 14, 231 (2021). https://doi.org/10.1186/s12920-021-01086-8

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  • DOI: https://doi.org/10.1186/s12920-021-01086-8