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

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

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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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Vestibular function of patients with profound deafness related to GJB2 mutation

By Kasai Misato   Hayashi Chieri   Iizuka Takashi   Inoshita Ayako   Kamiya Kazusaku   Okada Hiroko   Nakajima Yukinori   Kaga Kimitaka   Ikeda Katsuhisa  

Acta Oto-Laryngologica, Vol. 130, Iss. 9, 2010-09 ,pp. : 990-995

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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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