Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis
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), suggest...
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doaj-e07e02869c1341999b9a7131368625332021-05-11T11:27:48ZengNature Publishing GroupNature Communications2041-17232019-04-011011110.1038/s41467-019-09905-4Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalisElisavet Fotiou0Silvia Martin-Almedina1Michael A. Simpson2Shin Lin3Kristiana Gordon4Glen Brice5Giles Atton6Iona Jeffery7David C. Rees8Cyril Mignot9Julie Vogt10Tessa Homfray11Michael P. Snyder12Stanley G. Rockson13Steve Jeffery14Peter S. Mortimer15Sahar Mansour16Pia Ostergaard17Cardiovascular and Cell Sciences Institute, St. George’s University of LondonCardiovascular and Cell Sciences Institute, St. George’s University of LondonDepartment of Medical and Molecular Genetics, Division of Genetics and Molecular Medicine, Kings College London School of Medicine, Guy’s HospitalDivision of Cardiovascular Medicine, Stanford UniversityDepartment of Dermatology, St. George’s Healthcare NHS TrustSouth West Thames Regional Genetics Unit, St. George’s University of LondonSouth West Thames Regional Genetics Unit, St. George’s University of LondonPathology Department, St. George’s University of LondonDepartment of Haematological Medicine, King’s College London School of Medicine, King’s College HospitalDépartement de Génétique, APHP, GH Pitié-Salpêtrière, Centre de Référence des Déficiences Intellectuelles de Causes RaresWest Midlands Regional Genetics Service, Clinical Genetics Unit, Birmingham Women’s HospitalSouth West Thames Regional Genetics Unit, St. George’s University of LondonDepartment of Genetics, Stanford UniversityDivision of Cardiovascular Medicine, Stanford UniversityCardiovascular and Cell Sciences Institute, St. George’s University of LondonCardiovascular and Cell Sciences Institute, St. George’s University of LondonSouth West Thames Regional Genetics Unit, St. George’s University of LondonCardiovascular and Cell Sciences Institute, St. George’s University of LondonThis 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.https://doi.org/10.1038/s41467-019-09905-4 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
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 Michael P. Snyder Stanley G. Rockson Steve Jeffery Peter S. Mortimer Sahar Mansour Pia Ostergaard |
spellingShingle |
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 Michael P. Snyder Stanley G. Rockson Steve Jeffery Peter S. Mortimer Sahar Mansour Pia Ostergaard Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis Nature Communications |
author_facet |
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 Michael P. Snyder Stanley G. Rockson Steve Jeffery Peter S. Mortimer Sahar Mansour Pia Ostergaard |
author_sort |
Elisavet Fotiou |
title |
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis |
title_short |
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis |
title_full |
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis |
title_fullStr |
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis |
title_full_unstemmed |
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis |
title_sort |
author correction: novel mutations in piezo1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2019-04-01 |
description |
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. |
url |
https://doi.org/10.1038/s41467-019-09905-4 |
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