Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans

Buonocore, F., Kuehnen, P., Suntharalingham, J.P. et al. (24 more authors) (2017) Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans. JOURNAL OF CLINICAL INVESTIGATION, 127 (5). pp. 1700-1713. ISSN 0021-9738

Abstract

Metadata

Authors/Creators:
  • Buonocore, F.
  • Kuehnen, P.
  • Suntharalingham, J.P.
  • Del Valle, I.
  • Digweed, M.
  • Stachelscheid, H.
  • Khajavi, N.
  • Didi, M.
  • Brady, A.F.
  • Blankenstein, O.
  • Procter, A.M.
  • Dimitri, P.
  • Wales, J.K.H.
  • Ghirri, P.
  • Knoebl, D.
  • Strahm, B.
  • Erlacher, M.
  • Wlodarski, M.W.
  • Chen, W.
  • Kokai, G.K.
  • Anderson, G.
  • Morrogh, D.
  • Moulding, D.A.
  • McKee, S.A.
  • Niemeyer, C.M.
  • Grueters, A.
  • Achermann, J.C.
Copyright, Publisher and Additional Information: © 2017 The Author(s). Reproduced in accordance with the publisher's self-archiving policy.
Dates:
  • Published: 1 May 2017
  • Published (online): 27 March 2017
  • Accepted: 26 January 2017
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Sheffield Teaching Hospitals
Depositing User: Symplectic Sheffield
Date Deposited: 05 Jun 2017 12:28
Last Modified: 05 Jun 2017 12:28
Published Version: https://doi.org/10.1172/JCI91913
Status: Published
Publisher: American Society for Clinical Investigation
Refereed: Yes
Identification Number: https://doi.org/10.1172/JCI91913
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