@incollection{,
	
					
					
					FC0E4BD663E86F4D3C1C73230276ADAE
				,
	author={{Guilherme Machado deCarvalho} and {Tammy Fumiko MessiasTakara} and {Guilherme Machado deCarvalho} and {Priscila ZonziniRamos} and {Arthur MeninoCastilho} and {UNICAMP - Campinas University, SAo Paulo, Brazil}},
	journal={{Global Journal of Medical Research}},
	journal={{GJMR}}2249-46180975-588810.34257/GJMR,
	address={Cambridge, United States},
	publisher={Global Journals Organisation}1512328
}

@incollection{b0,
	
	
		,
	title={{Hearing loss: mechanisms revealed by genetics and cell biology}}
		,
	author={{
			AADror
		} and {
			KBAvraham
		}}
		
	
	
		,
	journal={{Annu Rev Genet}}
		
			43
			
			,
	year={2009}
		
	

}

@incollection{b1,
	
	
		,
	title={{Van Camp G. Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?}}
		,
	author={{
			NHilgert
		} and {
			RjhSmith
		}}
		
	
	
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	journal={{Mutat Res}}
		
			681
			
			,
	year={2009}
		
	

}

@book{b2,
	
	
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	title={{The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic}}
		,
	author={{
			HKokotas
		} and {
			MGrigoriadou
		} and {
			GSKorres
		} and {
			EFerekidou
		} and {
			EPapadopoulou
		} and {
			PNeou
		} and {
			AGiannoulia-Karantana
		} and {
			DKandiloros
		} and {
			SKorres
		} and {
			MBPetersen
		}}
		
		
		
		
		
		
		
		
		
		
	
	,
	note={sensorineural hearing loss}

}

@incollection{b3,
	
	
		,
	title={{}}
	
	
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	journal={{Biochem Biophys Res Commun}}
		
			390
			3
			
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	year={2009}
		
	

}

@incollection{b4,
	
	
		,
	title={{Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and nonsyndromic deafness}}
		,
	author={{
			TRPrezant
		} and {
			JVAgapian
		} and {
			MCBohlman
		} and {
			XBu
		} and {
			SÖztas
		}}
		
		
		
		
	
	
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@incollection{b5,
	
	
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	title={{}}
		
	
	
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			,
	year={2013}
		
	

}

@incollection{b6,
	
	
		,
	title={{Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene}}
		,
	author={{
			FDenoyelle
		} and {
			DWeil
		} and {
			MAMaw
		} and {
			SAWilcox
		} and {
			NJLench
		} and {
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		}}
		
		
		
		
		
	
	
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	journal={{Hum Mol Genet}}
		
			6
			
			,
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}

@incollection{b7,
	
	
		,
	title={{Connexin 26 mutations in hereditary non-syndromic sensorineural deafness}}
		,
	author={{
			DPKelsell
		} and {
			JDunlop
		} and {
			HPStevens
		} and {
			NJLench
		} and {
			JNLiang
		} and {
			GParry
		} and {
			RFMueller
		} and {
			IMLeigh
		}}
		
		
		
		
		
		
		
	
	
		,
	journal={{Nature}}
		
			387
			
			,
	year={1997}
		
	

}

@incollection{b8,
	
	
		,
	title={{Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study}}
		,
	author={{
			DelCastillo
		} and {
			IMoreno-Pelayo
		} and {
			MA
		} and {
			DelCastillo
		} and {
			FJBrownstein
		} and {
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		} and {
			S
		} and {
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		,
	journal={{Am J Hum Genet}}
		
			73
			
			,
	year={2003}
		
	

}

@incollection{b9,
	
	
		,
	title={{A novel deletion involving the connexin-30 gene, del(GJB6-D13S1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment}}
		,
	author={{
			DelCastillo
		} and {
			FJRodríguez-Ballesteros
		} and {
			MAlvarez
		} and {
			AHutchin
		} and {
			TLeonardi
		} and {
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		} and {
			CA
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		,
	journal={{J Med Genet}}
		
			42
			
			,
	year={2005}
		
	

}

@incollection{b10,
	
	
		,
	title={{Mitochondrial mutation A1555G (12S rRNA) and connexin 26 35delG mutation are frequent causes of deafness in Brazil}}
		,
	author={{
			RCMingroni-Netto
		} and {
			RSAbreu-Silva
		} and {
			MccBraga
		} and {
			KLezirovitz
		} and {
			Della-RosaVa
		}}
		
		
		
		
	
	
		,
	journal={{Am J Hum Genet}}
		
			69
			,
	year={2001}
		
	
	,
	note={suppl A2124}

}

@incollection{b11,
	
	
		,
	title={{Study of a Brazilian family presenting non-syndromic hearing loss with mitochondrial inheritance}}
		,
	author={{
			ACPupo
		} and {
			SPirana
		} and {
			MSpinelli
		} and {
			KLezirovitz
		} and {
			RCMingroni-Netto
		}}
		
		
		
		
	
	
		,
	journal={{Braz J Otorhinolaryngol}}
		
			74
			
			,
	year={2008}
		
	

}

@incollection{b12,
	
	
		,
	title={{Etiologic diagnosis of nonsyndromic genetic hearing loss in adult vs pediatric populations}}
		,
	author={{
			PJKing
		} and {
			XOuyang
		} and {
			LDu
		} and {
			DYan
		} and {
			SIAngeli
		}}
		
		
		
		
	
	
		,
	journal={{Otolaryngol Head Neck Surg}}
		
			147
			
			,
	year={2012}
		
	

}

@incollection{b13,
	
	
		,
	title={{The future role of genetic screening to detect newborns at risk of childhoodonset hearing loss}}
		,
	author={{
			LLPhillips
		} and {
			MBitner-Glindzicz
		} and {
			NLench
		} and {
			KSteel
		} and {
			CLangford
		} and {
			SJDawson
		}}
		
		
		
		
		
	
	
		,
	journal={{International J Audiol}}
		
			52
			
			,
	year={2013}
		
	

}

@incollection{b14,
	
	
		,
	title={{Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China}}
		,
	author={{
			QWei
		} and {
			SWang
		} and {
			JYao
		} and {
			YLu
		} and {
			ZChen
		} and {
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		}}
		
		
		
		
		
	
	
		,
	journal={{J Transl Med}}
		
			4
			11
			163
			,
	year={2013}
		
	

}

@incollection{b15,
	
	
		,
	title={{Prevalence and Clinical Features of the Mitochondrial m.1555AA>G Mutation in Taiwanese Patients with Idiopatic Sensorineural Hearing Loss and Association of Haplogroup F with Low Penetrance in Three Families}}
		,
	author={{
			CCWu
		} and {
			YHChiu
		} and {
			PJChen
		} and {
			CJHsu
		}}
		
		
		
	
	
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	journal={{Ear & Hearing}}
		
			28
			3
			
			,
	year={2007}
		
	

}

@book{b16,
	
	
		,
	title={{Mitochondrial COX2 G7598A Mutation May Have a Modifying Role in the Phenotypic Manifestation of Aminoglycoside Antibiotic-Induced Deafness Associated with 12S rRNA A1555G Mutation in a Han Chinese Pedigree}}
		,
	author={{
			TChen
		} and {
			QLiu
		} and {
			LJiang
		} and {
			CLiu
		} and {
			QOu
		}}
		
		
		
		
		
	

}

@incollection{b17,
	
	
		,
	title={{Infant hearing loss: from diagnosis to therapy}}
		,
	author={{
			GPaludetti
		} and {
			GConti
		} and {
			DiNardo
		} and {
			W
		} and {
			DeCorso
		} and {
			ERolesi
		} and {
			RPicciotti
		} and {
			PM
		}}
		
		
		
		
		
		
		
	
	
		,
	journal={{Acta Otorhinolaryngol Ital}}
		
			32
			
			,
	year={2012}
		
	

}

@incollection{b18,
	
	
		,
	title={{Pediatric BAHA in Italy: the "Bambino Gesu" Children´s Hospital´s experience}}
		,
	author={{
			PMarsella
		} and {
			AScorpecci
		} and {
			CPacifico
		}}
		
		
	
	
		,
	journal={{Eur Arch Otorhinolaryngol}}
		
			269
			
			,
	year={2012}
		
	

}

@incollection{b19,
	
	
		,
	title={{Totally implantable middle-ear device for rehabilitation os sensorineural hearing loss: preliminary experience with the Esteem, Envoy}}
		,
	author={{
			MBarbara
		} and {
			VManni
		} and {
			SMonini
		}}
		
		
	
	
		,
	journal={{Acta Otolaryngol}}
		
			129
			
			,
	year={2009}
		
	

}

@incollection{b20,
	
	
		,
	title={{Development of language and speech perception in congenitally, profoundly deaf children as a function of age at cochlear implantation}}
		,
	author={{
			MASvirsky
		} and {
			SWTeoh
		} and {
			HNeuburger
		}}
		
		
	
	
		,
	journal={{Audiol Neurootol}}
		
			9
			
			,
	year={2004}
		
	

}

@incollection{b21,
	
	
		,
	title={{Biotechnology in the Treatment of Sensorineural Hearing Loss:Foundations and Future of Hair Cell Regeneration}}
		,
	author={{
			MAParker
		}}
	
	
		,
	journal={{J Speech Lang Hear Res}}
		
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			6
			
			,
	year={2011}
		
	

}