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Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia.

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Bibliographic Details
Title: Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia.
Authors: Cornish N; Bristol Medical School., Aungraheeta MR; School of Cellular and Molecular Medicine, and., FitzGibbon L; School of Cellular and Molecular Medicine, and., Burley K; School of Cellular and Molecular Medicine, and., Alibhai D; Wolfson Bioimaging Facility, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom., Collins J; Department of Haematology, University of Cambridge, Cambridge, United Kingdom., Greene D; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge, United Kingdom.; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom; and., Downes K; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom; and., Westbury SK; School of Cellular and Molecular Medicine, and., Turro E; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge, United Kingdom.; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom; and.; NHS Blood and Transplant, Cambridge Biomedical Campus, Cambridge, United Kingdom., Mumford AD; School of Cellular and Molecular Medicine, and.
Corporate Authors: NIHR BioResource
Source: Blood advances [Blood Adv] 2020 Mar 10; Vol. 4 (5), pp. 920-924.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: American Society of Hematology Country of Publication: United States NLM ID: 101698425 Publication Model: Print Cited Medium: Internet ISSN: 2473-9537 (Electronic) Linking ISSN: 24739529 NLM ISO Abbreviation: Blood Adv Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2473-9537
DOI:10.1182/bloodadvances.2019001293