A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing

Poulter, JA, Smith, CEL, Murrillo, G et al. (9 more authors) (2015) A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing. Molecular Genetics & Genomic Medicine, 3 (6). pp. 543-549.

Abstract

Metadata

Authors/Creators:
  • Poulter, JA
  • Smith, CEL
  • Murrillo, G
  • Silva, S
  • Feather, S
  • Howell, M
  • Crinnion, L
  • Bonthron, DT
  • Carr, I
  • Watson, CM
  • Inglehearn, CF
  • Mighell, AJ
Copyright, Publisher and Additional Information: © 2015 The Authors. This is an open access article under the terms of the Creative Commons Attribution License (CC-BY 4.0), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Keywords: Amelogenesis imperfecta; CNVseq; namel renal syndrome; FAM20A
Dates:
  • Published: November 2015
  • Accepted: 11 June 2015
  • Published (online): 4 October 2015
Institution: The University of Leeds
Academic Units: 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 Medicine (Leeds) > Inst of Biomed & Clin Sciences (LIBACS) (Leeds) > Genetics (LIBACS) (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: 18 Jun 2015 14:33
Last Modified: 12 May 2016 08:44
Published Version: https://dx.doi.org/10.1002/mgg3.164
Status: Published
Publisher: Wiley
Identification Number: https://doi.org/10.1002/mgg3.164

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