Homozygous M34T mutation of the GJB2 gene associates with an autosomal recessive nonsyndromic sensorineural hearing impairment in Finnish families

By Löppönen Tuija   Dietz Aarno   Väisänen Marja-Leena   Valtonen Hannu   Kosunen Ari   Hyvärinen Antti   Ignatius Jaakko   Löppönen Heikki  

Acta Oto-Laryngologica, Vol. 132, Iss. 8, 2012-08 ,pp. : 862-873

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Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutations

By Moteki Hideaki   Naito Yasushi   Fujiwara Keizo   Kitoh Ryosuke   Nishio Shin-ya   Oguchi Kazuhiro   Takumi Yutaka   Usami Shin-ichi  

Acta Oto-Laryngologica, Vol. 131, Iss. 11, 2011-11 ,pp. : 1232-1236

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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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Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

By Ji Yu-bin   Han Dong-Yi   Lan Lan   Wang Da-Yong   Zong Liang   Zhao Fei-Fan   Liu Qiong   Benedict-Alderfer Cindy   Zheng Qing-yin   Wang Qiu-Ju  

Acta Oto-Laryngologica, Vol. 131, Iss. 2, 2011-02 ,pp. : 124-129

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Analysis of the presence of the GJB6 mutations in patients heterozygous for GJB2 mutation in Brazil

By Esteves Maria   Lima Isaac Myriam   Francisco Anete   Silva Junior Wilson   Ferreira Cristiane   Dell’Aringa Ana  

European Archives of Oto-Rhino-Laryngology, Vol. 271, Iss. 4, 2014-04 ,pp. : 695-699

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