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A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss
Noguchi, Yoshihiro, Yashima, Takatoshi, Hatanaka, Akio, Uzawa, Masamichi, Yasunami, Michio, Kimura, Akinori, Kitamura, KenVolume:
125
Language:
english
Journal:
Acta Oto-laryngologica
DOI:
10.1080/00016480510044232
Date:
January, 2005
File:
PDF, 179 KB
english, 2005