Mutation analysis of the Cx26, Cx30, and Cx31 genes in autosomal recessive nonsyndromic hearing impairment

By Gurtler Nicolas   Egenter Carole   Bosch Nemya   Plasilova Martina  

Acta Oto-Laryngologica, Vol. 128, Iss. 10, 2008-01 ,pp. : 1056-1062

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The Prevalence of Connexin 26 Mutations in the Swedish Population

By Hederstierna Christina   Möller Claes   Åhlman Henrik   Lundberg Rebecca   Von Döbeln Ulrika  

Audiological Medicine, Vol. 3, Iss. 3, 2005-09 ,pp. : 154-157

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Impaired membrane targeting and aberrant cellular localization of human Cx26 mutants associated with inherited recessive hearing loss

By Xiao Zian   Yang Zhongchun   Liu Xuezhong   Xie Dinghua  

Acta Oto-Laryngologica, Vol. 131, Iss. 1, 2011-01 ,pp. : 59-66

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The Effect of the Nasal Cycle on the Interpretation of Rhinomanometric Results in a Nasal Provocation Test

By Sipilä Jukka I.   Suonpää Jouko T.   Salmivalli Altti J.   Laippala Pekka  

American Journal of Rhinology, Vol. 4, Iss. 5, 1990-09 ,pp. : 179-184

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GJB2 (Connexin 26) gene mutations among hearing-impaired persons in a Swedish cohort

By Carlsson Per-Inge   Karltorp Eva   Carlsson-Hansén Eva   Åhlman Henrik   Möller Claes   VonDöbeln Ulrika  

Acta Oto-Laryngologica, Vol. 132, Iss. 12, 2012-12 ,pp. : 1301-1305

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