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Genotype analysis and identification of novel mutations in a multicentre cohort of patients with hereditary factor X deficiency.
Mitchell, Michael; Gattens, Michael; Kavakli, Kaan; Liesner, Ri; Payne, Jeanette; Norton, Miranda; Austin, Steven.
Affiliation
  • Mitchell M; Molecular Haemostasis & Thrombosis, Viapath Analytics LLP, St. Thomas' Hospital, London.
  • Gattens M; The Cambridge Haemophilia and Thrombophilia Centre, Cambridge University Hospitals, Cambridge, UK.
  • Kavakli K; Ege University Medicine Faculty, Izmir, Turkey.
  • Liesner R; Haemophilia Comprehensive Care Centre, Great Ormond Street Hospital, London.
  • Payne J; Department of Paediatric Haematology, Sheffield.
  • Norton M; Bio Products Laboratory Ltd., Elstree.
  • Austin S; St. George's Haemophilia Centre, St. George's University Hospitals NHS Foundation Trust, London, UK.
Blood Coagul Fibrinolysis ; 30(1): 34-41, 2019 Jan.
Article in En | MEDLINE | ID: mdl-30507709
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Factor X / Factor X Deficiency / Genotype / Mutation Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 2019 Document type: Article
Fulltext
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XML
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Factor X / Factor X Deficiency / Genotype / Mutation Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 2019 Document type: Article