The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency : a case series

Sun, M., Mueller, J.W., Gilligan, L.C. et al. (15 more authors) (2021) The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency : a case series. European Journal of Endocrinology, 185 (5). pp. 729-741. ISSN 0804-4643

Abstract

Metadata

Authors/Creators:
  • Sun, M.
  • Mueller, J.W.
  • Gilligan, L.C.
  • Taylor, A.E.
  • Shaheen, F.
  • Noczyńska, A.
  • T’Sjoen, G.
  • Denvir, L.
  • Shenoy, S.
  • Fulton, P.
  • Cheetham, T.D.
  • Gleeson, H.
  • Rahman, M.
  • Krone, N.P. ORCID logo https://orcid.org/0000-0002-3402-4727
  • Taylor, N.F.
  • Shackleton, C.H.L.
  • Arlt, W.
  • Idkowiak, J.
Copyright, Publisher and Additional Information: © 2021 The Authors. This work is licensed under a Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/).
Dates:
  • Accepted: 15 September 2021
  • Published (online): 11 October 2021
  • Published: 1 November 2021
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield)
Depositing User: Symplectic Sheffield
Date Deposited: 12 Nov 2021 07:57
Last Modified: 12 Nov 2021 07:57
Status: Published
Publisher: Bioscientifica
Refereed: Yes
Identification Number: https://doi.org/10.1530/eje-21-0152

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