This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Insights into phenotypic differences between humans and mice with p.T721M and other C-terminal variants of the SLC26A4 gene
Scientific Reports Open Access 25 October 2021
-
SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct
BMC Medical Genetics Open Access 02 July 2019
-
Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects
BMC Medical Genetics Open Access 08 May 2018
Access options
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Batsakis, J.G. & Nishiyama, R.H. Arch. Otolaryngol. 76, 401–406 (1962).
Reardon, W. & Trembath, R.C. J. Med. Genet. 33, 1037–1040 (1996).
Baldwin, C.T. et al. Hum. Mol. Genet 4, 1637–1642 (1995).
Hjelstuen, O.K. Analyst 120, 863–866 (1995).
Johnsen, T. et al. J. Laryngol. Otol. 101, 1187–1192 (1987).
Everett, L.A. et al. Nature Genet. 17, 411–422 (1997).
Gausden, E. et al. J. Med. Genet. 34, 126–129 (1997).
Arcand, P. et al. J. Otolaryngol. 20, 247–250 (1991).
Welsh, M.J. & Smith, A.E. Cell 73, 1251–1254 (1993).
Gibson, F. et al. Nature 374, 62–64 (1995).
Liu, X.Z. et al. Nature Genet. 16, 188–190 (1997).
Liu, X.Z. et al. Nature Genet. 17, 268–269 (1997).
Weil, D. et al. Nature Genet. 16, 191–193 (1997).
Author information
Authors and Affiliations
Corresponding authors
Rights and permissions
About this article
Cite this article
Li, X., Everett, L., Lalwani, A. et al. A mutation in PDS causes non-syndromic recessive deafness. Nat Genet 18, 215–217 (1998). https://doi.org/10.1038/ng0398-215
Issue Date:
DOI: https://doi.org/10.1038/ng0398-215
This article is cited by
-
ARNSHL gene identification: past, present and future
Molecular Genetics and Genomics (2022)
-
Identification of autosomal recessive nonsyndromic hearing impairment genes through the study of consanguineous and non-consanguineous families: past, present, and future
Human Genetics (2022)
-
Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss
Human Genetics (2022)
-
Insights into phenotypic differences between humans and mice with p.T721M and other C-terminal variants of the SLC26A4 gene
Scientific Reports (2021)
-
Gene therapy development in hearing research in China
Gene Therapy (2020)