[1] Nelson DI,Nelson RY,Concha-Barrientos M,et al. The global burden of occupational noise-induced hearing loss[J]. Am J Ind Med,2005,48(6):446-458. [2] Henderson D,Hamernik RP. Biologic bases of noise-induced hearing loss[J]. Occup Med State Art Rev,1995,10(3):513-534. [3] Sliwinska-Kowalska M,Pawelczyk M. Contribution of genetic factors to noise-induced hearing loss:a human studies review[J]. Mutat Res,2013,752(1):61-65. [4] Adhikary B,Ghosh S,Paul S,et al. Spectrum and frequency of GJB2,GJB6 and SLC26A4 gene mutations among non-syndromic hearing loss patients in eastern part of India[J]. Gene,2015,573(2):239-245. [5] Beck C,Pérez-álvarez JC,Sigruener A,et al. Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss[J]. Eur Arch Otorhinolaryngol, 2015,272(10):2765-2776. [6] Fang Y,Gu M,Wang C,et al. GJB2 as well as SLC26A4 gene mutations are prominent causes for congenital deafness[J]. Cell Biochem Biophys,2015,73(1):41-44. [7] Wangemann P. K+ cycling and the endocochlear potential[J]. Hear Res,2002,165(1):1-9. [8] Van Laer L,Carlsson PI,Ottschytsch N,et al. The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss[J]. Hum Mutat,2006, 27:786-795. [9] Naito T,Nishio SY,Iwasa Y,et al. Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort:genotype-phenotype correlations and a founder mutation[J]. PLoS One,2013, 8(5):e63231. [10] 谈柯宏,于德财,张娟,等. KCNQ4和GJB2基因多态性与职业噪声性听力损失的相关性研究[J]. 癌变·畸变·突变,2015,27(4):284-287. [11] Dai Z,Sun B,Huang S,et al. Correlation analysis of phenotype and genotype of GJB2 in patients with non-syndromic hearing loss in China[J]. Gene,2015,570(2):272-276. [12] Salman M,Bashir R,Imtiaz A,et al. Mutations of GJB2 encoding connexin 26 contribute to non-syndromic moderate and severe hearing loss in Pakistan[J]. Eur Arch Otorhinolaryngol, 2015. 272(8):2071-2075. [13] Tsukada K,Nishio S,Hattori M,et al. Ethnic-specific spectrum of GJB2 and SLC26A4 mutations their origin and a literature review[J]. Ann Otol Rhinol Laryngol,2015,124(1):61-76. [14] Terrinoni A,Codispoti A,Serra V,et al. Connexin 26(GJB2) mutations as a cause of the KID syndrome with hearing loss[J]. Biochem Biophys Res Commun,2010,395(1):25-30. [15] 程洪波. 遗传性非综合征型耳聋两种致病基因易感位点的关联分析[D]. 南京:南京医科大学,2008. [16] 李倩. 聋病遗传与环境相关高危因素的流行病学研究[D]. 北京:中国人民解放军医学院,2014. [17] Kokotas H,Van Laer L,Grigoriadou M,et al. Strong linkage disequilibrium for the frequent GJB 235delG mutation in the Greek population[J]. Am J Med Genet,2008,146(22):2879-2884. [18] Wei Q,Wang S,Yao J,et al. Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu province of China[J]. J Transl Med,2013,11(1):163. [19] Jiang H,Chen J,Shan XJ,et al. Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive nonsyndromic hearing loss[J]. Mol Med Report, 2014,10(1):379-386. [20] Grillo AP,de Oliveira FM,de Carvalho GQ,et al. Single nucleotide polymorphisms of the GJB2 and GJB6 genes are associated with autosomal recessive nonsyndromic hearing loss[J]. Biomed Res Int,2015,2015:318727. |