Phenotypic spectrum in osteogenesis imperfecta due to mutations in TMEM38B: unravelling a complex cellular defect.

Webb, E.A., Balasubramanian, M., Fratzl-Zelman, N. et al. (16 more authors) (2017) Phenotypic spectrum in osteogenesis imperfecta due to mutations in TMEM38B: unravelling a complex cellular defect. Journal of Clinical Endocrinology and Metabolism. ISSN 0021-972X

Abstract

Metadata

Authors/Creators:
  • Webb, E.A.
  • Balasubramanian, M.
  • Fratzl-Zelman, N.
  • Cabral, W.A.
  • Titheradge, H.
  • Alsaedi, A.
  • Saraff, V.
  • Vogt, J.
  • Cole, T.
  • Stewart, S.
  • Crabtree, N.J.
  • Sargent, B.M.
  • Gamsjaeger, S.
  • Paschalis, E.P.
  • Roschger, P.
  • Klaushofer, K.
  • Shaw, N.J.
  • Marini, J.C.
  • Högler, W.
Copyright, Publisher and Additional Information: © 2017 Endocrine Society. This is an author produced version of a paper subsequently published in Journal of Clinical Endocrinology and Metabolism. Uploaded in accordance with the publisher's self-archiving policy.
Keywords:
Dates:
  • Published (online): 16 March 2017
  • Accepted: 9 March 2017
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > School of Medicine (Sheffield)
Depositing User: Symplectic Sheffield
Date Deposited: 05 Apr 2017 10:35
Last Modified: 11 Apr 2017 17:12
Published Version: https://doi.org/10.1210/jc.2016-3766
Status: Published online
Publisher: Endocrine Society
Refereed: Yes
Identification Number: https://doi.org/10.1210/jc.2016-3766
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