Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

Johnson, B., Lowe, G.C., Futterer, J. et al. (31 more authors) (2016) Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects. Haematologica. ISSN 0390-6078

Abstract

Metadata

Authors/Creators:
  • Johnson, B.
  • Lowe, G.C.
  • Futterer, J.
  • Lordkipanidze', M.
  • MacDonald, D.
  • Simpson, M.A.
  • Sanchez Guiu', I.
  • Drake, S.
  • Bem, D.
  • Leo, V.
  • Fletcher, S.J.
  • Dawood, B.
  • Rivera, J.
  • Allsup, D.
  • Biss, T.
  • Bolton-Maggs, P.H.B.
  • Collins, P.
  • Curry, N.
  • Grimley, C.
  • James, B.
  • Makris, M.
  • Motwani, J.
  • Pavord, S.
  • Talks, K.
  • Thachil, J.
  • Wilde, J.
  • Williams, M.
  • Harrison, P.
  • Gissen, P.
  • Mundell, S.
  • Mumford, A.
  • Daly, M.E. https://orcid.org/0000-0002-4597-8921
  • Watson, S.P.
  • Morgan, N.V.
Copyright, Publisher and Additional Information: © 2016 Ferrata Storti Foundation. This is an author produced version of a paper subsequently published in Haematologica. Uploaded in accordance with the publisher's self-archiving policy.
Dates:
  • Published (online): 16 June 2016
  • Published: 16 June 2016
  • Accepted: 10 June 2016
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: 01 Aug 2016 13:14
Last Modified: 21 Mar 2018 19:30
Published Version: http://dx.doi.org/10.3324/haematol.2016.146316
Status: Published
Publisher: Ferrata Storti Foundation
Refereed: Yes
Identification Number: https://doi.org/10.3324/haematol.2016.146316

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