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Article

Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.

Annals of human genetics - 1 Nov 2017

Luo Jianfen, Bai Xiaohui, Zhang Fengguo, Xiao Yun, Gu Lintao, Han Yuechen, Fan Zhaomin, Li Jianfeng, Xu Lei, Wang Haibo

Abstract excerpt

The mutations of GJB2, SLC26A4, and mtDNA12SrRNA are the most common inherited causes of nonsyndromic sensorineural hearing loss (NSHL) in China, yet previous genetic screenings were mainly carried on patients with moderate-to-profound impairment. We aimed to detect the mutation frequencies in NSHL population within a more specified range of severity. Patients with profound NSHL who had undergone cochlear...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 28786104
DOI: 10.1111/ahg.12207

Genes

GJB2

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