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Variants of OTOF and PJVK Genes in Chinese Patients with Auditory Neuropathy Spectrum Disorder

BACKGROUND: Mutations in OTOF and PJVK genes cause DFNB9 and DFNB59 types of hearing loss, respectively. The patients carrying pathogenic mutations in either of these genes may show the typical phenotype of auditory neuropathy spectrum disorder (ANSD). The aim of the present study was to identify OT...

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Bibliografiske detaljer
Main Authors: Jian, Wang, Ying-ying, Fan, Shu-juan, Wang, Peng-Fei, Liang, Jin-ling, Wang, Jian-hua, Qiu
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2011
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3174136/
https://ncbi.nlm.nih.gov/pubmed/21935370
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0024000
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