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Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders
Authors:V. C. Leo  N. V. Morgan  D. Bem  M. L. Jones  G. C. Lowe  M. Lordkipanidzé  S. Drake  M. A. Simpson  P. Gissen  A. Mumford  S. P. Watson  M. E. Daly  the UK GAPP Study Group
Affiliation:1. Department of Cardiovascular Science, University of Sheffield Medical School, University of Sheffield, Sheffield, UK;2. Centre for Cardiovascular Sciences, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK;3. Schools of Physiology and Pharmacology and Cellular and Molecular Medicine, University of Bristol, Bristol, UK;4. Division of Genetics and Molecular Medicine, King's College London School of Medicine, Guy's Hospital, London, UK;5. Department of Genes, Development and Disease, Institute of Child Health, University College London, London, UK
Abstract:
Keywords:bioinformatics  bleeding  blood platelet disorders  high‐throughput DNA sequencing  platelets
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