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Correction: Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders
BMC Medical Genomics volume 17, Article number: 201 (2024)
The Original Article was published on 16 April 2024
Correction: BMC Med Genomics 17, 85 (2024)
https://doi.org/10.1186/s12920-024-01852-4
Following the publication of the Original Article [1], the authors reported an error in the placement of the plots during the manuscript preparation step. The authors accidentally placed the plots for Family HOU1842 in the Family of HOU4131, which resulted the duplication of Figure 1 Plots B and H and Supplementary Figure 2B and 5B.
Incorrect
Figure 1
Supplementary Figure 5
Correct
Figure 1
Supplementary Figure 5
The authors indicate that these errors do not affect any of the results nor the conclusions presented in the text of the study.
The Original Article has been corrected.
Reference
Bozkurt-Yozgatli, et al. Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders. BMC Med Genomics. 2024;17:85. https://doi.org/10.1186/s12920-024-01852-4.
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Bozkurt‑Yozgatli, T., Pehlivan, D., Gibbs, R.A. et al. Correction: Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders. BMC Med Genomics 17, 201 (2024). https://doi.org/10.1186/s12920-024-01968-7
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DOI: https://doi.org/10.1186/s12920-024-01968-7