Hemophilia B: Molecular pathogenesis and mutation analysis

Goodeve, A.C. (2015) Hemophilia B: Molecular pathogenesis and mutation analysis. Journal of Thrombosis and Haemostasis, 13 (7). pp. 1184-1195. ISSN 1538-7933

Abstract

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Authors/Creators:
  • Goodeve, A.C.
Copyright, Publisher and Additional Information: © 2015 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals, Inc. on behalf of International Society on Thrombosis and Haemostasis. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
Keywords: DNA Mutational Analysis; factor IX; genetic carrier detection; hemophilia B; prenatal diagnosis
Dates:
  • Published: 18 May 2015
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > School of Medicine (Sheffield) > Department of Cardiovascular Science
Depositing User: Symplectic Sheffield
Date Deposited: 28 Sep 2015 13:56
Last Modified: 03 Nov 2016 07:24
Published Version: https://doi.org/10.1111/jth.12958
Status: Published
Publisher: Wiley
Refereed: Yes
Identification Number: https://doi.org/10.1111/jth.12958

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