Correction: Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders
Tugce Bozkurt‑Yozgatli, Davut Pehlivan, Richard A. Gibbs, Ugur Sezerman, Jennifer E. Posey, James R. Lupski, Zeynep Coban‑Akdemir
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Click any figure to enlarge with its caption.
Figure 1
Figure 2
Figure 3
Figure 4Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsAdolescent and Pediatric Healthcare · Autism Spectrum Disorder Research · Genomics and Rare Diseases
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.