Author Correction: Complex de novo structural variants are an underestimated cause of rare disorders

Le résumé fourni par la source

In the version of this article initially published, there was a typographical error in the second paragraph of the Discussion section, where in the text now reading “In addition, 66 of 145 (46%) pathogenic SVs identified in our study were balanced rearrangements,” 66 of 145 (46%) originally read “51 of 151 (34%).” In Fig. 2g, the gene label “ SRRM2 ” was mistakenly placed to the right of the x -axis and is now realigned toward the center. In the first paragraph of the Results section, a related reference and associated discussion were missing. The text is now amended to include “Furthermore, 19 of the pathogenic dnSVs involving inversions were validated by an independent group [Pagnamenta, A. T. et al. The impact of inversions across 33,924 families with rare disease from a national genome sequencing project. Am. J. Hum. Genet . https://doi.org/10.1016/j.ajhg.2024.04.018 (2024)].” The changes are made in the HTML and PDF versions of the article.

Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.