LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss

Al-Amri, AH, Al Saegh, A, Al-Mamari, W et al. (10 more authors) (2019) LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. European Journal of Medical Genetics, 62 (12). 103592. ISSN 1769-7212

Abstract

Metadata

Authors/Creators:
Keywords: Deafness; Homozygosity mapping; Exome sequencing; LHFPL5
Dates:
  • Published: December 2019
  • Accepted: 22 November 2018
  • Published (online): 23 November 2018
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Biological Sciences (Leeds) > School of Biomedical Sciences (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 21 Mar 2019 11:07
Last Modified: 06 Dec 2019 16:46
Status: Published
Publisher: Elsevier
Identification Number: https://doi.org/10.1016/j.ejmg.2018.11.026

Download not available

A full text copy of this item is not currently available from White Rose Research Online

Share / Export

Statistics