Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

Naz, A. orcid.org/0000-0002-8747-5951, Biswas, A., Khan, T.N. et al. (7 more authors) (2017) Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population. Thrombosis Journal, 15 (24). ISSN 1477-9560

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Copyright, Publisher and Additional Information: © The Author(s). 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Keywords: Afibrinogenemia; Molecular modeling; FGA gene; Consanguinity; Inherited bleeding disorder
Dates:
  • Published: 12 September 2017
  • Accepted: 28 June 2017
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Cardiovascular Science (Sheffield)
The University of Sheffield > Sheffield Teaching Hospitals
Depositing User: Symplectic Sheffield
Date Deposited: 10 Jan 2018 14:42
Last Modified: 10 Jan 2018 14:42
Published Version: https://doi.org/10.1186/s12959-017-0143-3
Status: Published online
Publisher: BioMed Central
Refereed: Yes
Identification Number: https://doi.org/10.1186/s12959-017-0143-3
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