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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...

詳細記述

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書誌詳細
主要な著者: Jian, Wang, Ying-ying, Fan, Shu-juan, Wang, Peng-Fei, Liang, Jin-ling, Wang, Jian-hua, Qiu
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2011
主題:
オンライン・アクセス: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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