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BioMed Research International
Volume 2014, Article ID 746838, 6 pages
Research Article

Associations between GJB2, Mitochondrial 12S rRNA, SLC26A4 Mutations, and Hearing Loss among Three Ethnicities

1Department of Otolaryngology-Head and Neck Surgery, The Second Hospital of Lanzhou University, Lanzhou 730030, China
2Department of Otolaryngology-Head and Neck Surgery, Chinese People’s Liberation Army Institute of Otolaryngology, Chinese People’s Liberation Army General Hospital, Beijing 100039, China
3Health Department of Gansu Province, Lanzhou 730030, China

Received 27 February 2014; Accepted 11 March 2014; Published 2 April 2014

Academic Editor: Jareen Meinzen-Derr

Copyright © 2014 Wan Du et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [10 citations]

The following is the list of published articles that have cited the current article.

  • Ilaria Stanghellini, Elisabetta Genovese, Silvia Palma, Anna Ravani, Cristina Falcinelli, Maria Consolatrice Guarnaccia, and Antonio Percesepe, “New and Rare GJB2 Alleles in Patients with Nonsyndromic Sensorineural Hearing Impairment: A Genotype/Auditory Phenotype Correlation,” Genetic Testing and Molecular Biomarkers, vol. 18, no. 12, pp. 839–844, 2014. View at Publisher · View at Google Scholar
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