Hearing Loss and M.1555a>G Mitochondrial Mutation

Hearing Loss and M.1555a>G Mitochondrial Mutation

Guilherme Machado de Carvalho * §

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Universidade Estadual de Campinas (UNICAMP)

Hearing Loss and M.1555a>G Mitochondrial Mutation

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22 Cites in Article

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Amiel Dror,Karen Avraham (2009). Hearing Loss: Mechanisms Revealed by Genetics and Cell Biology.
Nele Hilgert,Richard Smith,Guy Van Camp (2009). Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?.
Haris Kokotas,Maria Grigoriadou,George Korres,Elisabeth Ferekidou,Eleftheria Papadopoulou,Polyxene Neou,Aglaia Giannoulia-Karantana,Dimitrios Kandiloros,Stavros Korres,Michael Petersen (2009). The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.
Toni Prezant,John Agapian,M Bohlman,Xiangdong Bu,Sitki Öztas,Wei-Qin Qiu,Kathleen Arnos,Gino Cortopassi,Lutfi Jaber,Jerome Rotter,Mordechai Shohat,Nathan Fischel-Ghodsian (1993). Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness.
(2013). MITOMAP: A Human Mitochondrial Genome Database.
F Denoyelle,D Weil,M Maw,S Wilcox,N Lench,D Allen-Powell,A Osborn,H Dahl,A Middleton,M Houseman,C Dode,S Marlin,A Boulila-Elgaied,M Grati,H Ayadi,S Benarab,P Bitoun,G Lina-Granade,J Godet,M Mustapha,J Loiselet,E El-Zir,A Aubois,A Joannard,J Levilliers,E-N Garabedian,R Mueller,R Mckinlay Gardner,C Petit (1997). Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene.
D Kelsell,J Dunlop,H Stevens,N Lench,J Liang,G Parry,R Mueller,I Leigh (1997). Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.
Ignacio Del Castillo,Miguel Moreno-Pelayo,Francisco Del Castillo,Zippora Brownstein,Sandrine Marlin,Quint Adina,David Cockburn,Arti Pandya,Kirby Siemering,G Chamberlin,Ester Ballana,Wim Wuyts,Andréa Maciel-Guerra,Araceli Álvarez,Manuela Villamar,Mordechai Shohat,Dvorah Abeliovich,Hans-Henrik M. Dahl,Xavier Estivill,Paolo Gasparini,Tim Hutchin,Walter Nance,Edi Sartorato,Richard Smith,Guy Van Camp,Karen Avraham,Christine Petit,Felipe Moreno (2003). Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study.
Del Castillo,F Rodríguez-Ballesteros,M Alvarez,A Hutchin,T Leonardi,E De Oliveira,C (2005). 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.
R Mingroni-Netto,R Abreu-Silva,Mcc Braga,K Lezirovitz,Della-Rosa Va (2001). Mitochondrial mutation A1555G (12S rRNA) and connexin 26 35delG mutation are frequent causes of deafness in Brazil.
Altair Pupo,Sulene Pirana,Mauro Spinelli,Karina Lezirovitz,Regina Netto,Lisandra Macedo (2008). Study of a Brazilian Family Presenting Non-syndromic hearing loss with mitochondrial inheritance.
Peter King,Xiaomei Ouyang,Lilin Du,Denise Yan,Simon Angeli,Xue Liu (2012). Etiologic Diagnosis of Nonsyndromic Genetic Hearing Loss in Adult vs Pediatric Populations.
L Phillips,M Bitner-Glindzicz,N Lench,K Steel,C Langford,S Dawson (2013). The future role of genetic screening to detect newborns at risk of childhoodonset hearing loss.
Qinjun Wei,Shuai Wang,Jun Yao,Yajie Lu,Zhibin Chen,Guangqian Xing,Xin Cao (2013). Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China.
C Wu,Y Chiu,P Chen,C Hsu (2007). 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.
Tianbin Chen,Qicai Liu,Ling Jiang,Can Liu,Qishui Ou (2013). 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.
C Angulo,J Gallo-Teran,B Senaris,A Fontalva,R Gonzalez-Aguado,J Fernandez-Luna (2011). Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycosides treatment.
G Paludetti,G Conti,Di Nardo,W,De Corso,E Rolesi,R Picciotti,P (2012). Infant hearing loss: from diagnosis to therapy.
Pasquale Marsella,Alessandro Scorpecci,Concettina Pacifico,Fabio Presuttari,Sergio Bottero (2012). Pediatric BAHA in Italy: the “Bambino Gesù” Children’s Hospital’s experience.
Maurizio Barbara,Vito Manni,Simonetta Monini (2009). Totally implantable middle ear device for rehabilitation of sensorineural hearing loss: preliminary experience with the Esteem®, Envoy.
Mario Svirsky,Su-Wooi Teoh,Heidi Neuburger (2004). Development of Language and Speech Perception in Congenitally, Profoundly Deaf Children as a Function of Age at Cochlear Implantation.
Mark Parker (2011). Biotechnology in the Treatment of Sensorineural Hearing Loss: Foundations and Future of Hair Cell Regeneration.

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Funding

No external funding was declared for this work.

Conflict of Interest

The authors declare no conflict of interest.

Ethical Approval

No ethics committee approval was required for this article type.

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Not applicable for this article.

How to Cite This Article

Guilherme Machado de Carvalho Machado de Carvalho. 1970. "Hearing Loss and M.1555a>G Mitochondrial Mutation". Global Journal of Medical Research - J: Dentistry & Otolaryngology GJMR-J Volume 15 (GJMR Volume 15 Issue J1).

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GJMR Volume 15 Issue J1

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Journal Specifications

Crossref Journal DOI 10.17406/gjmr

Print ISSN 0975-5888

e-ISSN 2249-4618

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GJMR-J Classification NLMC Code: WV 270

Published May 23, 2015

Version of record

v1.2

Issue date

May 23, 2015

Language

English

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