Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation

By Men Meichao   Jiang Lu   Wang Honghan   Liu Yalan   Hu Zhengmao   He Chufeng   Feng Yong  

Acta Oto-Laryngologica, Vol. 131, Iss. 9, 2011-09 ,pp. : 970-975

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Different Clinical Characteristics of Aminoglycoside-Induced Profound Deafness with and without the 1555 A→G Mitochondrial Mutation

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ORL, Vol. 63, Iss. 1, 2001-01 ,pp. : 25-30

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Sensorineural Hearing Loss and the 1555G Mitochondrial DNA Mutation

By Hutchin Tim  

Acta Oto-Laryngologica, Vol. 119, Iss. 1, 1999-04 ,pp. : 48-52

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Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)

By Usami Shin-ichi   Miyagawa Maiko   Nishio Shin-ya   Moteki Hideaki   Takumi Yutaka   Suzuki Mika   Kitano Yoko   Iwasaki Satoshi  

Acta Oto-Laryngologica, Vol. 132, Iss. 4, 2012-04 ,pp. : 377-384

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Isepamicin Sulfate-Induced Sensorineural Hearing Loss in Patients with the 1555 A→G Mitochondrial Mutation

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ORL, Vol. 60, Iss. 3, 1998-04 ,pp. : 164-169

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