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Martini A, Dafydd S, Read AP, Eds. Genes, Hearing, and Deafness: From Molecular Biology to Clinical Practice. Boca Raton, FL, USA: CRC Press, 2013.MartiniADafyddSReadAPBoca Raton, FL, USACRC Press2013Search in Google Scholar
Shearer AE, Smith RJ. Genetics: Advances in genetic testing for deafness. Curr Opin Pediatr. 2012; 24(6): 679-686.ShearerAESmithRJ.Genetics: Advances in genetic testing for deafness201224667968610.1097/MOP.0b013e3283588f5e369417823042251Search in Google Scholar
Shearer AE, Hildebrand MS, Sloan CM, Smith RJ. Deafness in the genomics era. Hear Res. 2011; 282(1-2):1-9.ShearerAEHildebrandMSSloanCMSmithRJ.Deafness in the genomics era20112821-21910.17077/etd.vlwonip2Search in Google Scholar
Daneshi A, Hassanzadeh S, Emamdjomeh H, Mohammadi SH, Arzhangi S, Farhadi M, et al. Prevalence of GJB2-associated deafness and outcomes of cochlear implantation in Iran. J Laryngol Otol. 2011; 125(05): 455-459.DaneshiAHassanzadehSEmamdjomehHMohammadiSHArzhangiSFarhadiMet al.Prevalence of GJB2-associated deafness and outcomes of cochlear implantation in Iran20111250545545910.1017/S002221511000299921281533Search in Google Scholar
Duman D, Tekin M. Autosomal recessive nonsyndromic deafness genes: A review. Front Biosci (Landmark Ed). 2012; 17: 2213-2236.DumanDTekinM.Autosomal recessive nonsyndromic deafness genes: A review2012172213223610.2741/4046368382722652773Search in Google Scholar
Ramsebner R, Ludwig M, Lucas T, de Jong D, Hamader G, del Castillo I, et al. Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter study. Otol Neurotol. 2013; 34(4): 650-656.RamsebnerRLudwigMLucasTde JongDHamaderGdel CastilloIet al.Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter study201334465065610.1097/MAO.0b013e31828d650123640091Search in Google Scholar
Yao YG, Salas A, Bravi CM, Bandelt HJ. A reappraisal of complete mtDNA variation in East Asian families with hearing impairment. Hum Genet. 2006; 119(5): 505-515.YaoYGSalasABraviCMBandeltHJ.A reappraisal of complete mtDNA variation in East Asian families with hearing impairment2006119550551510.1007/s00439-006-0154-916528519Search in Google Scholar
Yuan Y, You Y, Huang D, Cui J, Wang Y, Wang Q, et al. Comprehensive molecular etiology analysis of non-syndromic hearing impairment from typical areas in China. J Transl Med. 2009; 7(79): 1-12.YuanYYouYHuangDCuiJWangYWangQet al.Comprehensive molecular etiology analysis of non-syndromic hearing impairment from typical areas in China2009779112Search in Google Scholar
Ou QS, Cheng ZJ, Yang B, Jiang L, Chen J. Analysis of the ratio of mitchondrial DNA with A1555G mutant to wild type in deaf patients of Fujian province in China by a new method and its relationship with the severity of hearing loss. Chin Med J (Engl). 2011; 124(20): 3347-3352.OuQSChengZJYangBJiangLChenJ.Analysis of the ratio of mitchondrial DNA with A1555G mutant to wild type in deaf patients of Fujian province in China by a new method and its relationship with the severity of hearing loss20111242033473352Search in Google Scholar
Lu SY, Nishio S, Tsukada K, Oguchi T, Kobayashi K, Abe S, et al. Factors that affect hearing level in individuals with the mitochondrial 1555A.G mutation. Clin Genet 2009; 75(5): 480-484.LuSYNishioSTsukadaKOguchiTKobayashiKAbeSet al.Factors that affect hearing level in individuals with the mitochondrial 1555A.G mutation200975548048410.1111/j.1399-0004.2008.01138.x19475720Search in Google Scholar
Stephens D. Definitions, Protocols & Guidelines in Genetic Hearing Impairment. Audiological Terms. Letchworth, Hertfordshire, UK: Whurr Publishers, 2001.StephensD.Definitions, Protocols & Guidelines in Genetic Hearing ImpairmentLetchworth, Hertfordshire, UKWhurr Publishers2001Search in Google Scholar
Jin L, Yang A, Zhu Y, Zhao J, Wang X, Yang L, et al. Mitochondrial tRNA Ser (UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss. Biochem Biophys Res Comm. 2007; 361(1): 133-139.JinLYangAZhuYZhaoJWangXYangLet al.Mitochondrial tRNA Ser (UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss2007361113313910.1016/j.bbrc.2007.06.17117659260Search in Google Scholar
Chen B, Sun D, Yang L, Zhang C, Yang A, Zhu Y, et al. Mitochondrial ND5 T12338C, tRNA (Cys) T5802C, and tRNA (Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness associated 12S rRNA A1555G mutation in three Han Chinese pedigrees. Am J Med Genet A. 2008; 146(10): 1248-1258.ChenBSunDYangLZhangCYangAZhuYet al.Mitochondrial ND5 T12338C, tRNA (Cys) T5802C, and tRNA (Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness associated 12S rRNA A1555G mutation in three Han Chinese pedigrees2008146101248125810.1002/ajmg.a.3228518386806Search in Google Scholar
Gabriel H, Kupsch P, Sudendey J, Winterhager E, Jahnke K, Lautermann J. Mutations in the connexin26/GJB2 gene are the most common event in non syndromic hearing loss among the German population [J]. Hum Mutat. 2001; 17(6): 521-522.GabrielHKupschPSudendeyJWinterhagerEJahnkeKLautermannJ.Mutations in the connexin26/GJB2 gene are the most common event in non syndromic hearing loss among the German population [J]200117652152210.1002/humu.113811385713Search in Google Scholar
Gallant E, Francey L, Fetting H, Kaur M, Hakonarson H, Clark D, et al. Novel COCH mutation in a family with autosomal dominant late onset sensorineural hearing impairment and tinnitus. Am J Otolaryngol. 2013; 34(3): 230-235.GallantEFranceyLFettingHKaurMHakonarsonHClarkDet al.Novel COCH mutation in a family with autosomal dominant late onset sensorineural hearing impairment and tinnitus201334323023510.1016/j.amjoto.2012.11.00223374487Search in Google Scholar
Todt I, Hennies HC, Basta D, Ernst A. Vestibular dysfunction of patients with mutations of Connexin 26. Neuroreport. 2005; 16(11): 1179-1181.TodtIHenniesHCBastaDErnstA.Vestibular dysfunction of patients with mutations of Connexin 26200516111179118110.1097/00001756-200508010-0000916012344Search in Google Scholar
Thatcher A, Le Prell C, Miller J, Green G. ACEMg supplementation ameliorates progressive Connexin 26 hearing loss in a child. Int J Pediatr Otorhinolaryngol. 2014; 78(3): 563-565.ThatcherALe PrellCMillerJGreenG.ACEMg supplementation ameliorates progressive Connexin 26 hearing loss in a child201478356356510.1016/j.ijporl.2013.12.03024439969Search in Google Scholar
Ma T, Xue X, Dai P, Cao X, Chi J, Deng J, et al. Epidemiological studies on mtDNA 12S rRNA A1555G mutation of 10 non syndromic hearing loss families in Yunnan province. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012; 26(13): 581-585.MaTXueXDaiPCaoXChiJDengJet al.Epidemiological studies on mtDNA 12S rRNA A1555G mutation of 10 non syndromic hearing loss families in Yunnan province20122613581585Search in Google Scholar
Lu J, Li Z, Zhu Y, Yang A, Li R, Zheng J, et al. Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss. Mitochondrion. 2010; 10(4): 380-390.LuJLiZZhuYYangALiRZhengJet al.Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss201010438039010.1016/j.mito.2010.01.007287465920100600Search in Google Scholar
Wang X, Lu J, Zhu Y, Yang A, Yang L, Li R, et al. Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families. Pharmacogenet Genom. 2008; 18(12): 1059-1070.WangXLuJZhuYYangAYangLLiRet al.Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families200818121059107010.1097/FPC.0b013e3283131661290537818820594Search in Google Scholar
Lu J, Qian Y, Li Z, Yang A, Zhu Y, Li R, et al. Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555 A>G mutation. Mitochondrion. 2010; 10(1): 69-81.LuJQianYLiZYangAZhuYLiRet al.Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555 A>G mutation2010101698110.1016/j.mito.2009.09.007278774619818876Search in Google Scholar