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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Detalles Bibliográficos
Autores principales: Jian, Wang, Ying-ying, Fan, Shu-juan, Wang, Peng-Fei, Liang, Jin-ling, Wang, Jian-hua, Qiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3174136/
https://www.ncbi.nlm.nih.gov/pubmed/21935370
http://dx.doi.org/10.1371/journal.pone.0024000

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3174136/
https://www.ncbi.nlm.nih.gov/pubmed/21935370
http://dx.doi.org/10.1371/journal.pone.0024000

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