A missense variant in specificity protein 6 (SP6) is associated with amelogenesis imperfecta

Smith, C orcid.org/0000-0001-8320-5105, Whitehouse, L, Poulter, J orcid.org/0000-0003-2048-5693 et al. (8 more authors) (2020) A missense variant in specificity protein 6 (SP6) is associated with amelogenesis imperfecta. Human Molecular Genetics. ISSN 0964-6906

Abstract

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Authors/Creators:
Dates:
  • Accepted: 4 March 2020
  • Published (online): 13 March 2020
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Biological Sciences (Leeds) > School of Molecular and Cellular Biology (Leeds) > Biological Chemistry (Leeds)
The University of Leeds > Faculty of Biological Sciences (Leeds) > School of Molecular and Cellular Biology (Leeds) > Crystallography (Leeds)
The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Dentistry (Leeds) > Oral Surgery (Leeds)
The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Dentistry (Leeds) > School of Dentistry Visitors (Leeds)
The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Institute of Rheumatology & Musculoskeletal Medicine (LIRMM) (Leeds) > Inflammatory Arthritis (Leeds)
Funding Information:
FunderGrant number
Pathological Society of Great Britain & IrelandPES 2017 03 01
Wellcome Trust093113/A/10/Z
Wellcome Trust062164/Z/00/Z
Wellcome Trust105615/Z/14/Z
Depositing User: Symplectic Publications
Date Deposited: 10 Mar 2020 09:58
Last Modified: 27 Mar 2020 14:31
Status: Published online
Publisher: Oxford University Press
Identification Number: https://doi.org/10.1093/hmg/ddaa041

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