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

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Bibliographic Details
Published in:Acta oto-laryngologica 2005-11, Vol.125 (11), p.1189-1194
Main Authors: NOGUCHI, Yoshihiro, YASHIMA, Takatoshi, HATANAKA, Akio, UZAWA, Masamichi, YASUNAMI, Michio, KIMURA, Akinori, KITAMURA, Ken
Format: Article
Language:English
Subjects:
Biological and medical sciences
Complex syndromes
Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology
Medical genetics
Medical sciences
Non tumoral diseases
Otorhinolaryngology. Stomatology
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ISSN:0001-6489
1651-2251
DOI:10.1080/00016480510044232