Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family

Al-Amri, A, Saegh, AA, Al-Mamari, W et al. (6 more authors) (2016) Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. American Journal of Medical Genetics Part A, 170 (7). pp. 1826-1831. ISSN 1552-4825

Abstract

Metadata

Authors/Creators:
  • Al-Amri, A
  • Saegh, AA
  • Al-Mamari, W
  • El-Asrag, ME
  • Ivorra, JL
  • Cardno, AG
  • Inglehearn, CF
  • Clapcote, SJ
  • Ali, M
Copyright, Publisher and Additional Information: © 2016, Wiley. This is the peer reviewed version of the following article: "Al-Amri A, Saegh AA, Al-Mamari W, El-Asrag ME, Ivorra JL, Cardno AG, Inglehearn CF, Clapcote SJ, Ali M. 2016. Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. Am J Med Genet Part A 170A:1826–1831" which has been published in final form at http://dx.doi.org/10.1002/ajmg.a.37690. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: intellectual disability; exome sequencing; TUSC3
Dates:
  • Published: July 2016
  • Accepted: 17 April 2016
  • Published (online): 5 May 2016
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Biological Sciences (Leeds) > School of Biomedical Sciences (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: 20 Jul 2016 09:00
Last Modified: 17 Jul 2017 14:26
Published Version: http://dx.doi.org/10.1002/ajmg.a.37690
Status: Published
Publisher: Wiley
Identification Number: https://doi.org/10.1002/ajmg.a.37690

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