Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme

By Chinetti Viviana   Iossa Sandra   Auletta Gennaro   Corvino Virginia   De Luca Maria   De Falco Francesca   Giannini Pasquale   Lilli Giorgio   Malesci Rita   Riccardi Pasquale   Marciano Elio   Franzè Annamaria  

International Journal of Audiology, Vol. 50, Iss. 12, 2011-12 ,pp. : 866-870

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GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in East Greenland

By Homøe Preben   Koch Anders   Rendtorff Nanna Dahl   Lodahl Marianne   Andersen Ture   Andersen Stig   Eiberg Hans   Nielsen Inge-Merete   Tranebjærg Lisbeth  

International Journal of Audiology, Vol. 51, Iss. 6, 2012-06 ,pp. : 433-436

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Determination of the carrier frequencies of selected GJB2 mutations in the Korean population

By Kim Shin Young   Lee Bom Yi   Lim Ji Hyae   Ryu Hyun Mee   Yang Jae Hyug   Chung Jin Hoon   Han Ho Won   Park So Yeon  

International Journal of Audiology, Vol. 50, Iss. 10, 2011-10 ,pp. : 694-698

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Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort

By Cama Elona   Melchionda Salvatore   Palladino Teresa   Carella Massimo   Santarelli Rosamaria   Genovese Elisabetta   Benettazzo Filippo   Zelante Leopoldo   Arslan Edoardo  

International Journal of Audiology, Vol. 48, Iss. 1, 2009-01 ,pp. : 12-17

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Spectrum and frequency of GJB2 mutations in a cohort of 264 Portuguese nonsyndromic sensorineural hearing loss patients

By Matos Tiago Daniel  

International Journal of Audiology, Vol. 52, Iss. 7, 2013-07 ,pp. : 466-471

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