Author
Listed:
- Elisavet Fotiou
(St. George’s University of London)
- Silvia Martin-Almedina
(St. George’s University of London)
- Michael A. Simpson
(Guy’s Hospital)
- Shin Lin
(Stanford University
Stanford University)
- Kristiana Gordon
(St. George’s Healthcare NHS Trust)
- Glen Brice
(St. George’s University of London)
- Giles Atton
(St. George’s University of London)
- Iona Jeffery
(St. George’s University of London)
- David C. Rees
(King’s College Hospital)
- Cyril Mignot
(Centre de Référence des Déficiences Intellectuelles de Causes Rares)
- Julie Vogt
(Birmingham Women’s Hospital)
- Tessa Homfray
(St. George’s University of London)
- Michael P. Snyder
(Stanford University)
- Stanley G. Rockson
(Stanford University)
- Steve Jeffery
(St. George’s University of London)
- Peter S. Mortimer
(St. George’s University of London)
- Sahar Mansour
(St. George’s University of London)
- Pia Ostergaard
(St. George’s University of London)
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.
Suggested Citation
Elisavet Fotiou & Silvia Martin-Almedina & Michael A. Simpson & Shin Lin & Kristiana Gordon & Glen Brice & Giles Atton & Iona Jeffery & David C. Rees & Cyril Mignot & Julie Vogt & Tessa Homfray & Mich, 2019.
"Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis,"
Nature Communications, Nature, vol. 10(1), pages 1-1, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09905-4
DOI: 10.1038/s41467-019-09905-4
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