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Audiological Medicine Volume 5, 2007 - Issue 3
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Original

Connexin 26 gene: Defining the role of the V1531 mutation

Veronica I. Guerci Genetica Medica, Dipartimento di Scienze della Riproduzione e dello Sviluppo, University of Trieste
,
Domenico L. Grasso Otorhinolaryngology Unit, IRCCS Burlo Garofolo Children Hospital, Trieste
,
Marcello Morgutti S.C. Genetica Medica, IRCCS Burlo Garofolo Children Hospital, Trieste
,
Antonio Amoroso Transplantation Immunology Service, San Giovanni Battista Hospital, Turin
,
Paola D'Andrea Dipartimento di Biochimica, Biofisica e Chimica delle Macromolecole, University of Trieste, Italy
,
Massimiliano Bicego Dipartimento di Biochimica, Biofisica e Chimica delle Macromolecole, University of Trieste, Italy
&
Paolo Gasparini Genetica Medica, Dipartimento di Scienze della Riproduzione e dello Sviluppo, University of Trieste; S.C. Genetica Medica, IRCCS Burlo Garofolo Children Hospital, TriesteCorrespondence[email protected]
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Pages 200-206 | Published online: 11 Jul 2009

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Tiago Daniel Matos, Helena Simões-Teixeira, Helena Caria, Ana Cláudia Gonçalves, Joana Chora, Maria do Céu Correia, Carla Moura, Helena Rosa, Luísa Monteiro, Assunção O’Neill, Óscar Dias, Mário Andrea & Graça Fialho. (2013) Spectrum and frequency of GJB2 mutations in a cohort of 264 Portuguese nonsyndromic sensorineural hearing loss patients. International Journal of Audiology 52:7, pages 466-471.
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Articles from other publishers (1)

Tiago D. MatosHelena Simões-TeixeiraHelena CariaHelena RosaAssunção O'NeillGraça Fialho. (2010) The Controversial p.Arg127His Mutation in GJB2 : Report on Three Portuguese Hearing Loss Family Cases . Genetic Testing and Molecular Biomarkers 14:1, pages 141-144.
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