Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.
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| Title: | Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis. |
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| Authors: | Fotiou E; Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK., Martin-Almedina S; Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK., Simpson MA; Department of Medical and Molecular Genetics, Division of Genetics and Molecular Medicine, Kings College London School of Medicine, Guy's Hospital, London, SE1 9RY, UK., Lin S; Division of Cardiovascular Medicine, Stanford University, Stanford, California, 94305, USA.; Department of Genetics, Stanford University, Stanford, California, 94305, USA., Gordon K; Department of Dermatology, St. George's Healthcare NHS Trust, London, SW17 0QT, UK., Brice G; South West Thames Regional Genetics Unit, St. George's University of London, London, SW17 0RE, UK., Atton G; South West Thames Regional Genetics Unit, St. George's University of London, London, SW17 0RE, UK., Jeffery I; Pathology Department, St. George's University of London, London, SW17 0RE, UK., Rees DC; Department of Haematological Medicine, King's College London School of Medicine, King's College Hospital, London, SE5 9RS, UK., Mignot C; Département de Génétique, APHP, GH Pitié-Salpêtrière, Centre de Référence des Déficiences Intellectuelles de Causes Rares, 75013, Paris, France., Vogt J; West Midlands Regional Genetics Service, Clinical Genetics Unit, Birmingham Women's Hospital, Birmingham, B15 2TG, UK., Homfray T; South West Thames Regional Genetics Unit, St. George's University of London, London, SW17 0RE, UK., Snyder MP; Department of Genetics, Stanford University, Stanford, California, 94305, USA., Rockson SG; Division of Cardiovascular Medicine, Stanford University, Stanford, California, 94305, USA., Jeffery S; Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK., Mortimer PS; Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK., Mansour S; South West Thames Regional Genetics Unit, St. George's University of London, London, SW17 0RE, UK., Ostergaard P; Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK. posterga@sgul.ac.uk. |
| Source: | Nature communications [Nat Commun] 2019 Apr 26; Vol. 10 (1), pp. 1951. Date of Electronic Publication: 2019 Apr 26. |
| Publication Type: | Published Erratum |
| Journal Info: | Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 31028252 AccessLevel: 2 PubTypeId: unknown PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Fotiou+E%22">Fotiou E</searchLink>; Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK.<br /><searchLink fieldCode="AU" term="%22Martin-Almedina+S%22">Martin-Almedina S</searchLink>; Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK.<br /><searchLink fieldCode="AU" term="%22Simpson+MA%22">Simpson MA</searchLink>; Department of Medical and Molecular Genetics, Division of Genetics and Molecular Medicine, Kings College London School of Medicine, Guy's Hospital, London, SE1 9RY, UK.<br /><searchLink fieldCode="AU" term="%22Lin+S%22">Lin S</searchLink>; Division of Cardiovascular Medicine, Stanford University, Stanford, California, 94305, USA.; Department of Genetics, Stanford University, Stanford, California, 94305, USA.<br /><searchLink fieldCode="AU" term="%22Gordon+K%22">Gordon K</searchLink>; Department of Dermatology, St. George's Healthcare NHS Trust, London, SW17 0QT, UK.<br /><searchLink fieldCode="AU" term="%22Brice+G%22">Brice G</searchLink>; South West Thames Regional Genetics Unit, St. George's University of London, London, SW17 0RE, UK.<br /><searchLink fieldCode="AU" term="%22Atton+G%22">Atton G</searchLink>; South West Thames Regional Genetics Unit, St. George's University of London, London, SW17 0RE, UK.<br /><searchLink fieldCode="AU" term="%22Jeffery+I%22">Jeffery I</searchLink>; Pathology Department, St. George's University of London, London, SW17 0RE, UK.<br /><searchLink fieldCode="AU" term="%22Rees+DC%22">Rees DC</searchLink>; Department of Haematological Medicine, King's College London School of Medicine, King's College Hospital, London, SE5 9RS, UK.<br /><searchLink fieldCode="AU" term="%22Mignot+C%22">Mignot C</searchLink>; Département de Génétique, APHP, GH Pitié-Salpêtrière, Centre de Référence des Déficiences Intellectuelles de Causes Rares, 75013, Paris, France.<br /><searchLink fieldCode="AU" term="%22Vogt+J%22">Vogt J</searchLink>; West Midlands Regional Genetics Service, Clinical Genetics Unit, Birmingham Women's Hospital, Birmingham, B15 2TG, UK.<br /><searchLink fieldCode="AU" term="%22Homfray+T%22">Homfray T</searchLink>; South West Thames Regional Genetics Unit, St. George's University of London, London, SW17 0RE, UK.<br /><searchLink fieldCode="AU" term="%22Snyder+MP%22">Snyder MP</searchLink>; Department of Genetics, Stanford University, Stanford, California, 94305, USA.<br /><searchLink fieldCode="AU" term="%22Rockson+SG%22">Rockson SG</searchLink>; Division of Cardiovascular Medicine, Stanford University, Stanford, California, 94305, USA.<br /><searchLink fieldCode="AU" term="%22Jeffery+S%22">Jeffery S</searchLink>; Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK.<br /><searchLink fieldCode="AU" term="%22Mortimer+PS%22">Mortimer PS</searchLink>; Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK.<br /><searchLink fieldCode="AU" term="%22Mansour+S%22">Mansour S</searchLink>; South West Thames Regional Genetics Unit, St. George's University of London, London, SW17 0RE, UK.<br /><searchLink fieldCode="AU" term="%22Ostergaard+P%22">Ostergaard P</searchLink>; Cardiovascular and Cell Sciences Institute, St. George's University of London, Cranmer Terrace, London, SW17 0RE, UK. posterga@sgul.ac.uk. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101528555%22">Nature communications</searchLink> [Nat Commun] 2019 Apr 26; Vol. 10 (1), pp. 1951. <i>Date of Electronic Publication: </i>2019 Apr 26. – Name: TypePub Label: Publication Type Group: TypPub Data: Published Erratum – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Pub%2E+Group%22">Nature Pub. Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101528555 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2041-1723 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2220411723%22">20411723 </searchLink><i>NLM ISO Abbreviation: </i>Nat Commun <i>Subsets: </i>PubMed not MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=31028252 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/s41467-019-09905-4 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1951 Titles: – TitleFull: Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Fotiou E – PersonEntity: Name: NameFull: Martin-Almedina S – PersonEntity: Name: NameFull: Simpson MA – PersonEntity: Name: NameFull: Lin S – PersonEntity: Name: NameFull: Gordon K – PersonEntity: Name: NameFull: Brice G – PersonEntity: Name: NameFull: Atton G – PersonEntity: Name: NameFull: Jeffery I – PersonEntity: Name: NameFull: Rees DC – PersonEntity: Name: NameFull: Mignot C – PersonEntity: Name: NameFull: Vogt J – PersonEntity: Name: NameFull: Homfray T – PersonEntity: Name: NameFull: Snyder MP – PersonEntity: Name: NameFull: Rockson SG – PersonEntity: Name: NameFull: Jeffery S – PersonEntity: Name: NameFull: Mortimer PS – PersonEntity: Name: NameFull: Mansour S – PersonEntity: Name: NameFull: Ostergaard P IsPartOfRelationships: – BibEntity: Dates: – D: 26 M: 04 Text: 2019 Apr 26 Type: published Y: 2019 Identifiers: – Type: issn-electronic Value: 2041-1723 Numbering: – Type: volume Value: 10 – Type: issue Value: 1 Titles: – TitleFull: Nature communications Type: main |
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