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Correction

Correction: DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease

  • Hong Xia,
  • Xiangjun Huang,
  • Sheng Deng,
  • Hongbo Xu,
  • Yan Yang,
  • Xin Liu,
  • Lamei Yuan,
  • Hao Deng
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There is an error in the third sentence of the first paragraph of the Discussion. The correct sentence is: Subsequently compound heterozygous variants, c.12363C>G (p. Tyr4121*) and c.13531_*36del (p.Ala4511_Ala4516delinsGln), in the DNAH11 gene were identified in a family with PCD, including a patient with SI.

Additionally, in Table 1, the columns Ethnicity, Sequence variants # and PCD phenotypes are incorrectly formatted. Please see the correct version of Table 1 here.

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Table 1. Clinical phenotypes of individuals with DNAH11 compound heterozygous variants.

https://doi.org/10.1371/journal.pone.0315965.t001

Reference

  1. 1. Xia H, Huang X, Deng S, Xu H, Yang Y, Liu X, et al. (2021) DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease. PLOS ONE 16(6): e0252786. pmid:34133440

Citation: Xia H, Huang X, Deng S, Xu H, Yang Y, Liu X, et al. (2024) Correction: DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease. PLoS ONE 19(12): e0315965. https://doi.org/10.1371/journal.pone.0315965

Published: December 12, 2024

Copyright: © 2024 Xia et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.