Correction to: Genetics in Medicine: doi: https://doi.org/10.1038/s41436-018-0281-4
The original version of this Article contained an error in the top left of Figure 2: the number 1 on the y-axis had been changed to 0 during the typesetting process. This has now been corrected in both the PDF and HTML versions of the Article.
In addition, this Article was originally published without the accompanying Supplementary Table 1. This file is now available in the HTML version of the Article; the PDF was correct from the time of publication.
Author information
Authors and Affiliations
Consortia
Corresponding author
Additional information
These authors are jointly first: Matthew Neil Wakeling and Thomas William Laver
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Wakeling, M.N., Laver, T.W., Wright, C.F. et al. Correction: Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian disease. Genet Med 21, 766 (2019). https://doi.org/10.1038/s41436-018-0357-1
Published:
Version of record:
Issue date:
DOI: https://doi.org/10.1038/s41436-018-0357-1
This article is cited by
-
Exome sequencing reveals broad genetic heterogeneity for neuromuscular disorders in consanguineous Pakistani Families
European Journal of Human Genetics (2025)
-
Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human gene
Human Genomics (2023)