Mutations in EPHB4 cause human venous valve aplasia.

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Bibliographic Details
Title: Mutations in EPHB4 cause human venous valve aplasia.
Authors: Lyons O; Academic Department of Vascular Surgery, Section of Vascular Risk and Surgery, School of Cardiovascular Medicine and Sciences, BHF Centre of Research Excellence, King's College London, St. Thomas' Hospital, London, United Kingdom., Walker J; Academic Department of Vascular Surgery, Section of Vascular Risk and Surgery, School of Cardiovascular Medicine and Sciences, BHF Centre of Research Excellence, King's College London, St. Thomas' Hospital, London, United Kingdom., Seet C; Academic Department of Vascular Surgery, Section of Vascular Risk and Surgery, School of Cardiovascular Medicine and Sciences, BHF Centre of Research Excellence, King's College London, St. Thomas' Hospital, London, United Kingdom., Ikram M; Academic Department of Vascular Surgery, Section of Vascular Risk and Surgery, School of Cardiovascular Medicine and Sciences, BHF Centre of Research Excellence, King's College London, St. Thomas' Hospital, London, United Kingdom., Kuchta A; Department of Ultrasonic Angiology, Guy's & St. Thomas' NHS Foundation Trust, London, United Kingdom., Arnold A; Department of Ultrasonic Angiology, Guy's & St. Thomas' NHS Foundation Trust, London, United Kingdom., Hernández-Vásquez M; Rudbeck Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Sweden., Frye M; Rudbeck Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Sweden., Vizcay-Barrena G; Centre for Ultrastructural Imaging, King's College London, London, United Kingdom., Fleck RA; Centre for Ultrastructural Imaging, King's College London, London, United Kingdom., Patel AS; Academic Department of Vascular Surgery, Section of Vascular Risk and Surgery, School of Cardiovascular Medicine and Sciences, BHF Centre of Research Excellence, King's College London, St. Thomas' Hospital, London, United Kingdom., Padayachee S; Department of Ultrasonic Angiology, Guy's & St. Thomas' NHS Foundation Trust, London, United Kingdom., Mortimer P; Molecular and Clinical Sciences Research Institute, St. George's University of London, London, United Kingdom., Jeffery S; Molecular and Clinical Sciences Research Institute, St. George's University of London, London, United Kingdom., Berland S; Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway., Mansour S; Molecular and Clinical Sciences Research Institute, St. George's University of London, London, United Kingdom.; South West Thames Regional Genetics Service, St. George's Hospital, London, United Kingdom., Ostergaard P; Molecular and Clinical Sciences Research Institute, St. George's University of London, London, United Kingdom., Makinen T; Rudbeck Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Sweden., Modarai B; Academic Department of Vascular Surgery, Section of Vascular Risk and Surgery, School of Cardiovascular Medicine and Sciences, BHF Centre of Research Excellence, King's College London, St. Thomas' Hospital, London, United Kingdom., Saha P; Academic Department of Vascular Surgery, Section of Vascular Risk and Surgery, School of Cardiovascular Medicine and Sciences, BHF Centre of Research Excellence, King's College London, St. Thomas' Hospital, London, United Kingdom., Smith A; Academic Department of Vascular Surgery, Section of Vascular Risk and Surgery, School of Cardiovascular Medicine and Sciences, BHF Centre of Research Excellence, King's College London, St. Thomas' Hospital, London, United Kingdom.
Source: JCI insight [JCI Insight] 2021 Sep 22; Vol. 6 (18). Date of Electronic Publication: 2021 Sep 22.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 101676073 Publication Model: Electronic Cited Medium: Internet ISSN: 2379-3708 (Electronic) Linking ISSN: 23793708 NLM ISO Abbreviation: JCI Insight Subsets: MEDLINE
Database: MEDLINE Ultimate
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