Mutation of the EYA1 Gene in Patients with Branchio-oto Syndrome

By Yashima Takatoshi   Noguchi Yoshihiro   Ishikawa Kinya   Mizusawa Hidehiro   Kitamura Ken  

Acta Oto-Laryngologica, Vol. 123, Iss. 2, 2003-01 ,pp. : 279-282

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Phenotypic consequences in a Japanese family having branchio-oto-renal syndrome with a novel frameshift mutation in the gene EYA1

By Matsunaga Tatsuo   Okada Michiyo   Usami Shin-Ichi   Okuyama Torayuki  

Acta Oto-Laryngologica, Vol. 127, Iss. 1, 2007-01 ,pp. : 98-104

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Audiovestibular findings in a branchio-oto syndrome patient with a SIX1 mutation

By Noguchi Yoshihiro   Ito Taku   Nishio Ayako   Honda Keiji   Kitamura Ken  

Acta Oto-Laryngologica, Vol. 131, Iss. 4, 2011-04 ,pp. : 413-418

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A Comparative Study of Eya1 and Eya4 Protein Function and Its Implication in Branchio-oto-renal Syndrome and DFNA10

By Zhang Yuzhou   Knosp Boyd   Maconochie Mark   Friedman Rick   Smith Richard  

JARO - Journal of the Association for Research in Otolaryngology, Vol. 5, Iss. 3, 2004-09 ,pp. : 295-304

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

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

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

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