Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss

By Yao Gendong   Chen Dingli   Wang Huijun   Li Shouxia   Zhang Jin   Feng Zhixing   Guo Lili   Yang Zhiming   Yang Sujun   Sun Caixia   Zhang Xiaofang   Ma Duan  

Acta Oto-Laryngologica, Vol. 133, Iss. 8, 2013-08 ,pp. : 833-841

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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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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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Commentary on the question of genotype-phenotype correlations in genetic hearing impairment

By Read Andrew  

Audiological Medicine, Vol. 2, Iss. 4, 2004-12 ,pp. : 259-261

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Col11a1 and col11a2 mRNA expression in the developing mouse Cochlea: Implications for the correlation of hearing loss phenotype with mutant type XI collagen genotype

By Shpargel Karl   Makishima Tomoko   Griffith Andrew  

Acta Oto-Laryngologica, Vol. 124, Iss. 3, 2004-03 ,pp. : 242-248

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