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. 2024 Aug 7;17:201. doi: 10.1186/s12920-024-01968-7

Correction: Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders

Tugce Bozkurt‑Yozgatli 1,2, Davut Pehlivan 3,4,5,6, Richard A Gibbs 7,8, Ugur Sezerman 1,9, Jennifer E Posey 7, James R Lupski 3,6,7,8,, Zeynep Coban‑Akdemir 2,7,
PMCID: PMC11308470  PMID: 39113026

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

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Supplementary Figure 5

graphic file with name 12920_2024_1968_Figb_HTML.jpg

Correct

Figure 1

graphic file with name 12920_2024_1968_Figc_HTML.jpg

Supplementary Figure 5

graphic file with name 12920_2024_1968_Figd_HTML.jpg

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.

Contributor Information

James R. Lupski, Email: jlupski@bcm.edu

Zeynep Coban‑Akdemir, Email: Zeynep.H.CobanAkdemir@uth.tmc.edu.

Reference

  • 1.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. 10.1186/s12920-024-01852-4. 10.1186/s12920-024-01852-4 [DOI] [PMC free article] [PubMed] [Google Scholar]

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