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Prevalence of Mutations in the GJB2, SLC26A4, GJB3, and MT-RNR1 Genes in 103 Children with Sensorineural Hearing Loss in Shaoxing, China

机译：103名儿童GJB2，SLC26A4，GJB3和MT-RNR1基因中突变的患病率在绍兴绍兴感官听力损失中的103名儿童中

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Hong Yu; Dan Liu; Jingqun Yang; Zhiqiang Wu;
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1. Comparative study of mutation spectrums of MT-RNR1 m.1555A＞G,GJB2, and SLC26A4 between familial and sporadic patients with nonsyndromic sensorineural hearing loss in Chinese Han [J] . Li Qian, Ji Yubin, Han Bing, 中华医学杂志（英文版） . 2014,第018期

机译：中国汉族非症状性感音神经性聋家庭和散发患者MT-RNR1 m.1555A＞ G，GJB2和SLC26A4突变谱的比较研究
2. Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China. [J] . Ji YB, Han DY, Lan L, Acta Oto-Laryngologica . 2011,第2期

机译：中国非综合征性感音神经性听力丧失的门诊患者线粒体DNA12SrRNA A1555G，GJB2和SLC26A4突变的分子流行病学分析。
3. Sensorineural hearing loss caused by mutations in two alleles of both GJB2 and SLC26A4 genes [J] . HuangS., HanD., WangG., International journal of pediatric otorhinolaryngology . 2013,第3期

机译：GJB2和SLC26A4基因的两个等位基因突变引起的感觉神经性听力损失
4. Functional consequences of missense mutation in the GJB2 gene associated with non-synclromic hearing loss [C] . Lee Kyu Yup, Choi Soo-Young, Lin Xi, Asia Pacific Symposium on Cochlear Implant and Related SciencesAsia Pacific Symposium on Cochlear Implant and Related Sciences . 2009

机译：与非辛瘤性听力损失相关的GJB2基因畸形突变的功能后果
5. Association between Uncoupling Protein 2 Gene Ala55val Polymorphism and Sudden Sensorineural Hearing Loss [D] . Koide Yusuke, 小出悠介 2019

机译：解偶联蛋白2基因Ala55val多态性与突然的感音神经性听力丧失之间的关联。
6. Prevalence of Mutations in GJB2 SLC26A4 and mtDNA in Children with Severe or Profound Sensorineural Hearing Loss in Southwestern China [O] . Jie Qing, Yuan Zhou, Ruosha Lai, -1

机译：西南地区严重或深感神经性听力丧失儿童的GJB2SLC26A4和mtDNA突变发生率
7. Prevalence of Mutations in GJB2, SLC26A4, and mtDNA in Children with Severe or Profound Sensorineural Hearing Loss in Southwestern China [O] . Jie Qing, Yuan Zhou, Ruosha Lai, 2015

机译：中国西南部严重或深远的感觉神经听力损失的儿童GJB2，SLC26A4和MTDNA中的突变患病率

Prevalence of Mutations in the GJB2, SLC26A4, GJB3, and MT-RNR1 Genes in 103 Children with Sensorineural Hearing Loss in Shaoxing, China

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