Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations

De La Dure-Molla, M, Quentric, M, Yamaguti, PM et al. (6 more authors) (2014) Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations. Orphanet Journal of Rare Diseases, 9 (1). 84. ISSN 1750-1172

Abstract

Metadata

Authors/Creators:
  • De La Dure-Molla, M
  • Quentric, M
  • Yamaguti, PM
  • Acevedo, A-C
  • Mighell, AJ
  • Vikkula, M
  • Huckert, M
  • Berdal, A
  • Bloch-Zupan, A
Copyright, Publisher and Additional Information: © 2014 de la Dure-Molla et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Keywords: Enamel Renal Syndrome (ERS); Amelogenesis Imperfecta and Gingival Fibromatosis syndrome (AIFGS); Enamel Dysplasia with Hamartomatous atypical Follicular Hyperplasia Syndrome (EDHFH); Amelogenesis Imperfecta; Enamel defect; Delayed tooth eruption; Intra-pulpal calcification; Gingival hyperplasia; FAM20A
Dates:
  • Published: 14 June 2014
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Dentistry (Leeds) > Oral Surgery (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 23 Oct 2014 09:49
Last Modified: 23 Oct 2014 09:49
Published Version: http://dx.doi.org/10.1186/1750-1172-9-84
Status: Published
Publisher: BioMed Central
Identification Number: https://doi.org/10.1186/1750-1172-9-84
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