SORA

Advancing, promoting and sharing knowledge of health through excellence in teaching, clinical practice and research into the prevention and treatment of illness

Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Fotiou, E; Martin-Almedina, S; Simpson, MA; Lin, S; Gordon, K; Brice, G; Atton, G; Jeffery, I; Rees, DC; Mignot, C; et al. Fotiou, E; Martin-Almedina, S; Simpson, MA; Lin, S; Gordon, K; Brice, G; Atton, G; Jeffery, I; Rees, DC; Mignot, C; Vogt, J; Homfray, T; Snyder, MP; Rockson, SG; Jeffery, S; Mortimer, PS; Mansour, S; Ostergaard, P (2019) Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis. Nat Commun, 10. p. 1951. ISSN 2041-1723 https://doi.org/10.1038/s41467-019-09905-4
SGUL Authors: Ostergaard, Pia

[img]
Preview
PDF Published Version
Available under License Creative Commons Attribution.

Download (246kB) | Preview

Abstract

This Article contains an error in the last sentence of the 'Variant analysis suggests they are pathogenic' section of the Results, which incorrectly reads 'No truncated PIEZO1 protein products were identified in western blot analysis in GLD1:II.3 and GLD2:II.2 (Fig. 2, Supplementary Fig. 6), suggesting that the truncated protein is not stable and therefore degraded.' This should read 'No full-size PIEZO1 protein products were identified in western blot analysis in GLD1:II.3 and GLD2:II.2 (Fig. 2, Supplementary Fig. 6); the three nonsense mutations are predicted to lead to premature termination of the protein, hence it is possible that those truncated proteins will be non-functional or even unstable and degraded.' The error has not been fixed in the PDF or HTML versions of the Article.

Item Type: Article
Additional Information: 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/. © The Author(s) 2019 Correction to https://doi.org/10.1038/ncomms9085 | http://openaccess.sgul.ac.uk/107589/
Keywords: MD Multidisciplinary
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Nat Commun
ISSN: 2041-1723
Language: eng
Dates:
DateEvent
26 April 2019Published
Publisher License: Creative Commons: Attribution 4.0
PubMed ID: 31028252
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/110847
Publisher's version: https://doi.org/10.1038/s41467-019-09905-4

Actions (login required)

Edit Item Edit Item