A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss

Author： Noguchi Yoshihiro Yashima Takatoshi Hatanaka Akio Uzawa Masamichi Yasunami Michio Kimura Akinori Kitamura Ken

Publisher： Informa Healthcare

ISSN： 0001-6489

Source： Acta Oto-Laryngologica, Vol.125, Iss.11, 2005-11, pp. : 1189-1194

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