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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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Detaylı Bibliyografya
Asıl Yazarlar: Jian, Wang, Ying-ying, Fan, Shu-juan, Wang, Peng-Fei, Liang, Jin-ling, Wang, Jian-hua, Qiu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2011
Konular:
Online Erişim: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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