Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta

Poulter, JA, El-Sayed, W, Shore, RC et al. (3 more authors) (2013) Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta. European Journal of Human Genetics, 22. 132 - 135. ISSN 1018-4813

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Authors/Creators:
  • Poulter, JA
  • El-Sayed, W
  • Shore, RC
  • Kirkham, J
  • Inglehearn, CF
  • Mighell, AJ
Copyright, Publisher and Additional Information: (c) 2014 Macmillan Publishers Limited All rights reserved. This work is licensed under a Creative Commons. Attribution-NonCommercial-NoDerivs 3.0 Unported License.
Keywords: amelogenesis; amelogenesis imperfecta; LAMB3; laminin-5
Dates:
  • Published: 1 May 2013
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Dentistry (Leeds) > Oral Biology (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) > Institute of Molecular Medicine (LIMM) (Leeds) > Section of Opthalmology and Neurosciences (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 21 May 2013 10:54
Last Modified: 16 Jan 2018 06:21
Published Version: http://dx.doi.org/10.1038/ejhg.2013.76
Status: Published
Publisher: Nature Publishing Group
Identification Number: https://doi.org/10.1038/ejhg.2013.76
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