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International Journal of Audiology Volume 41, 2002 - Issue 2
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Original Article

Connexin 26 preverbal hearing impairment: Mutation prevalence and heterozygosity in a selected population: Problemas auditivos preverbales por Conexina 26: Prevalencia de mutacion y heterocigosidad en una población seleccionada

Eva Orzan Department of Otosurgery, University Hospital, Padova, ItalyCorrespondence[email protected]
,
Alessandra Murgia Department of Paediatrics, University Hospital, Padova, Italy
,
Roberta Polli Department of Paediatrics, University Hospital, Padova, Italy
,
Maddalena Martella Department of Paediatrics, University Hospital, Padova, Italy
,
Alberto Mazzai Department of Clinical and Experimental Medicine, University Hospital, Padova, Italy
,
Franco Zacchello Department of Paediatrics, University Hospital, Padova, Italy
&
Gregorio Babighian Department of Otosurgery, University Hospital, Padova, Italy
 show all
Pages 120-124 | Received 03 Apr 2001, Accepted 20 Jun 2001, Published online: 07 Jul 2009

Citations (6)

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Read on this site (2)

Deepika Gopalarao, William J. Kimberling, Walt Jesteadt, Philip M. Kelley, Kathryn L. Beauchaine & Edward S. Cohn. (2008) Is hearing loss due to mutations in the Connexin 26 gene progressive?. International Journal of Audiology 47:1, pages 11-20.
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Stacey A. Apps, Wayne A. Rankin & Andrew P. Kurmis. (2007) Connexin 26 mutations in autosomal recessive deafness disorders: A review. International Journal of Audiology 46:2, pages 75-81.
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Articles from other publishers (4)

Dylan K. Chan & Kay W. Chang. (2014) GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype. The Laryngoscope 124:2, pages E34-E53.
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Olga Šterna, Natālija Proņina, Ieva Grīnfelde, Sandra Kušķe, Astrīda Krūmiņa, Rita Lugovska & Aigars Pētersons. (2009) Spectrum and Frequency of the GJB2 Gene Mutations Among Latvian Patients with Prelingual Nonsyndromic Hearing Loss. Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences. 63:4-5, pages 198-203.
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James E. Saunders, Sharon Vaz, John H. Greinwald, James Lai, Leonor Morin & Karen Mojica. (2007) Prevalence and Etiology of Hearing Loss in Rural Nicaraguan Children. The Laryngoscope 117:3, pages 387-398.
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Delphine Feldmann, Françoise Denoyelle, Pierre Chauvin, Eréa‐Noël Garabédian, Rémy Couderc, Sylvie Odent, Alain Joannard, Sébastien Schmerber, Bruno Delobel, Jacques Leman, Hubert Journel, Hélène Catros, Cédric Le Maréchal, Hélène Dollfus, Marie‐Madeleine Eliot, Jean‐Pierre Delaunoy, Albert David, Catherine Calais, Valérie Drouin‐Garraud, Marie‐Françoise Obstoy, Didier Bouccara, Olivier Sterkers, Patrice Tran Ba Huy, Cyril Goizet, Françoise Duriez, Florence Fellmann, Jocelyne Hélias, Jacqueline Vigneron, Bétina Montaut, Patricia Lewin, Christine Petit & Sandrine Marlin. (2004) Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: Genotypic and phenotypic analysis . American Journal of Medical Genetics Part A 127A:3, pages 263-267.
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